[{"has_accepted_license":"1","publication":"Angewandte Chemie International Edition","month":"12","oa_version":"Published Version","language":[{"iso":"eng"}],"type":"journal_article","date_published":"2017-12-04T00:00:00Z","tmp":{"name":"Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)","image":"/images/cc_by_nc.png","short":"CC BY-NC (4.0)","legal_code_url":"https://creativecommons.org/licenses/by-nc/4.0/legalcode"},"oa":1,"publication_identifier":{"issn":["1433-7851"]},"status":"public","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","file":[{"file_id":"7362","creator":"dernst","relation":"main_file","access_level":"open_access","date_updated":"2020-07-14T12:47:55Z","content_type":"application/pdf","file_name":"2017_AngChemieInternat_Schafzahl.pdf","date_created":"2020-01-26T14:58:07Z","file_size":1013492,"checksum":"3c5b1e51954554dffb13c7d58f69836c"}],"issue":"49","author":[{"full_name":"Schafzahl, Lukas","first_name":"Lukas","last_name":"Schafzahl"},{"last_name":"Mahne","first_name":"Nika","full_name":"Mahne, Nika"},{"first_name":"Bettina","last_name":"Schafzahl","full_name":"Schafzahl, Bettina"},{"last_name":"Wilkening","first_name":"Martin","full_name":"Wilkening, Martin"},{"first_name":"Christian","last_name":"Slugovc","full_name":"Slugovc, Christian"},{"full_name":"Borisov, Sergey M.","first_name":"Sergey M.","last_name":"Borisov"},{"id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425","first_name":"Stefan Alexander","last_name":"Freunberger","orcid":"0000-0003-2902-5319","full_name":"Freunberger, Stefan Alexander"}],"_id":"7289","intvolume":"        56","title":"Singlet oxygen during cycling of the aprotic sodium-O2 battery","article_processing_charge":"No","date_created":"2020-01-15T12:15:05Z","publication_status":"published","file_date_updated":"2020-07-14T12:47:55Z","quality_controlled":"1","page":"15728-15732","article_type":"original","publisher":"Wiley","year":"2017","citation":{"apa":"Schafzahl, L., Mahne, N., Schafzahl, B., Wilkening, M., Slugovc, C., Borisov, S. M., &#38; Freunberger, S. A. (2017). Singlet oxygen during cycling of the aprotic sodium-O2 battery. <i>Angewandte Chemie International Edition</i>. Wiley. <a href=\"https://doi.org/10.1002/anie.201709351\">https://doi.org/10.1002/anie.201709351</a>","ama":"Schafzahl L, Mahne N, Schafzahl B, et al. Singlet oxygen during cycling of the aprotic sodium-O2 battery. <i>Angewandte Chemie International Edition</i>. 2017;56(49):15728-15732. doi:<a href=\"https://doi.org/10.1002/anie.201709351\">10.1002/anie.201709351</a>","chicago":"Schafzahl, Lukas, Nika Mahne, Bettina Schafzahl, Martin Wilkening, Christian Slugovc, Sergey M. Borisov, and Stefan Alexander Freunberger. “Singlet Oxygen during Cycling of the Aprotic Sodium-O2 Battery.” <i>Angewandte Chemie International Edition</i>. Wiley, 2017. <a href=\"https://doi.org/10.1002/anie.201709351\">https://doi.org/10.1002/anie.201709351</a>.","ieee":"L. Schafzahl <i>et al.</i>, “Singlet oxygen during cycling of the aprotic sodium-O2 battery,” <i>Angewandte Chemie International Edition</i>, vol. 56, no. 49. Wiley, pp. 15728–15732, 2017.","mla":"Schafzahl, Lukas, et al. “Singlet Oxygen during Cycling of the Aprotic Sodium-O2 Battery.” <i>Angewandte Chemie International Edition</i>, vol. 56, no. 49, Wiley, 2017, pp. 15728–32, doi:<a href=\"https://doi.org/10.1002/anie.201709351\">10.1002/anie.201709351</a>.","short":"L. Schafzahl, N. Mahne, B. Schafzahl, M. Wilkening, C. Slugovc, S.M. Borisov, S.A. Freunberger, Angewandte Chemie International Edition 56 (2017) 15728–15732.","ista":"Schafzahl L, Mahne N, Schafzahl B, Wilkening M, Slugovc C, Borisov SM, Freunberger SA. 2017. Singlet oxygen during cycling of the aprotic sodium-O2 battery. Angewandte Chemie International Edition. 56(49), 15728–15732."},"date_updated":"2021-01-12T08:12:47Z","abstract":[{"text":"Aprotic sodium–O2 batteries require the reversible formation/dissolution of sodium superoxide (NaO2) on cycling. Poor cycle life has been associated with parasitic chemistry caused by the reactivity of electrolyte and electrode with NaO2, a strong nucleophile and base. Its reactivity can, however, not consistently explain the side reactions and irreversibility. Herein we show that singlet oxygen (1O2) forms at all stages of cycling and that it is a main driver for parasitic chemistry. It was detected in‐ and ex‐situ via a 1O2 trap that selectively and rapidly forms a stable adduct with 1O2. The 1O2 formation mechanism involves proton‐mediated superoxide disproportionation on discharge, rest, and charge below ca. 3.3 V, and direct electrochemical 1O2 evolution above ca. 3.3 V. Trace water, which is needed for high capacities also drives parasitic chemistry. Controlling the highly reactive singlet oxygen is thus crucial for achieving highly reversible cell operation.","lang":"eng"}],"day":"04","doi":"10.1002/anie.201709351","ddc":["540"],"extern":"1","volume":56},{"article_type":"original","publisher":"Wiley","page":"12394-12397","quality_controlled":"1","title":"Orthogonal light-induced self-assembly of nanoparticles using differently substituted azobenzenes","intvolume":"        54","publication_status":"published","article_processing_charge":"No","date_created":"2023-08-01T09:44:19Z","author":[{"full_name":"Manna, Debasish","first_name":"Debasish","last_name":"Manna"},{"first_name":"Thumu","last_name":"Udayabhaskararao","full_name":"Udayabhaskararao, Thumu"},{"first_name":"Hui","last_name":"Zhao","full_name":"Zhao, Hui"},{"id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b","last_name":"Klajn","first_name":"Rafal","full_name":"Klajn, Rafal"}],"issue":"42","_id":"13393","pmid":1,"scopus_import":"1","extern":"1","volume":54,"abstract":[{"text":"Precise control of the self-assembly of selected components within complex mixtures is a challenging goal whose realization is important for fabricating novel nanomaterials. Herein we show that by decorating the surfaces of metallic nanoparticles with differently substituted azobenzenes, it is possible to modulate the wavelength of light at which the self-assembly of these nanoparticles is induced. Exposing a mixture of two types of nanoparticles, each functionalized with a different azobenzene, to UV or blue light induces the selective self-assembly of only one type of nanoparticles. Irradiation with the other wavelength triggers the disassembly of the aggregates, and the simultaneous self-assembly of nanoparticles of the other type. By placing both types of azobenzenes on the same nanoparticles, we created unique materials (“frustrated” nanoparticles) whose self-assembly is induced irrespective of the wavelength of the incident light.","lang":"eng"}],"doi":"10.1002/anie.201502419","day":"01","external_id":{"pmid":["25959725"]},"date_updated":"2023-08-07T12:58:29Z","year":"2015","citation":{"mla":"Manna, Debasish, et al. “Orthogonal Light-Induced Self-Assembly of Nanoparticles Using Differently Substituted Azobenzenes.” <i>Angewandte Chemie International Edition</i>, vol. 54, no. 42, Wiley, 2015, pp. 12394–97, doi:<a href=\"https://doi.org/10.1002/anie.201502419\">10.1002/anie.201502419</a>.","short":"D. Manna, T. Udayabhaskararao, H. Zhao, R. Klajn, Angewandte Chemie International Edition 54 (2015) 12394–12397.","ista":"Manna D, Udayabhaskararao T, Zhao H, Klajn R. 2015. Orthogonal light-induced self-assembly of nanoparticles using differently substituted azobenzenes. Angewandte Chemie International Edition. 54(42), 12394–12397.","ama":"Manna D, Udayabhaskararao T, Zhao H, Klajn R. Orthogonal light-induced self-assembly of nanoparticles using differently substituted azobenzenes. <i>Angewandte Chemie International Edition</i>. 2015;54(42):12394-12397. doi:<a href=\"https://doi.org/10.1002/anie.201502419\">10.1002/anie.201502419</a>","apa":"Manna, D., Udayabhaskararao, T., Zhao, H., &#38; Klajn, R. (2015). Orthogonal light-induced self-assembly of nanoparticles using differently substituted azobenzenes. <i>Angewandte Chemie International Edition</i>. Wiley. <a href=\"https://doi.org/10.1002/anie.201502419\">https://doi.org/10.1002/anie.201502419</a>","ieee":"D. Manna, T. Udayabhaskararao, H. Zhao, and R. Klajn, “Orthogonal light-induced self-assembly of nanoparticles using differently substituted azobenzenes,” <i>Angewandte Chemie International Edition</i>, vol. 54, no. 42. Wiley, pp. 12394–12397, 2015.","chicago":"Manna, Debasish, Thumu Udayabhaskararao, Hui Zhao, and Rafal Klajn. “Orthogonal Light-Induced Self-Assembly of Nanoparticles Using Differently Substituted Azobenzenes.” <i>Angewandte Chemie International Edition</i>. Wiley, 2015. <a href=\"https://doi.org/10.1002/anie.201502419\">https://doi.org/10.1002/anie.201502419</a>."},"language":[{"iso":"eng"}],"keyword":["General Chemistry","Catalysis"],"month":"10","oa_version":"None","publication":"Angewandte Chemie International Edition","status":"public","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","publication_identifier":{"issn":["1433-7851"],"eissn":["1521-3773"]},"date_published":"2015-10-01T00:00:00Z","type":"journal_article"},{"language":[{"iso":"eng"}],"page":"4312-4317","quality_controlled":"1","article_type":"original","publisher":"Wiley","author":[{"first_name":"Peixiang","last_name":"Ma","full_name":"Ma, Peixiang"},{"full_name":"Haller, Jens D.","last_name":"Haller","first_name":"Jens D."},{"full_name":"Zajakala, Jérémy","last_name":"Zajakala","first_name":"Jérémy"},{"full_name":"Macek, Pavel","first_name":"Pavel","last_name":"Macek"},{"first_name":"Astrid C.","last_name":"Sivertsen","full_name":"Sivertsen, Astrid C."},{"full_name":"Willbold, Dieter","first_name":"Dieter","last_name":"Willbold"},{"first_name":"Jérôme","last_name":"Boisbouvier","full_name":"Boisbouvier, Jérôme"},{"last_name":"Schanda","first_name":"Paul","full_name":"Schanda, Paul","orcid":"0000-0002-9350-7606","id":"7B541462-FAF6-11E9-A490-E8DFE5697425"}],"issue":"17","publication":"Angewandte Chemie International Edition","_id":"8460","title":"Probing transient conformational states of proteins by solid-state R1ρ relaxation-dispersion NMR spectroscopy","month":"03","intvolume":"        53","publication_status":"published","oa_version":"None","date_created":"2020-09-18T10:08:53Z","article_processing_charge":"No","extern":"1","status":"public","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","volume":53,"date_published":"2014-03-18T00:00:00Z","type":"journal_article","date_updated":"2021-01-12T08:19:25Z","citation":{"apa":"Ma, P., Haller, J. D., Zajakala, J., Macek, P., Sivertsen, A. C., Willbold, D., … Schanda, P. (2014). Probing transient conformational states of proteins by solid-state R1ρ relaxation-dispersion NMR spectroscopy. <i>Angewandte Chemie International Edition</i>. Wiley. <a href=\"https://doi.org/10.1002/anie.201311275\">https://doi.org/10.1002/anie.201311275</a>","ama":"Ma P, Haller JD, Zajakala J, et al. Probing transient conformational states of proteins by solid-state R1ρ relaxation-dispersion NMR spectroscopy. <i>Angewandte Chemie International Edition</i>. 2014;53(17):4312-4317. doi:<a href=\"https://doi.org/10.1002/anie.201311275\">10.1002/anie.201311275</a>","chicago":"Ma, Peixiang, Jens D. Haller, Jérémy Zajakala, Pavel Macek, Astrid C. Sivertsen, Dieter Willbold, Jérôme Boisbouvier, and Paul Schanda. “Probing Transient Conformational States of Proteins by Solid-State R1ρ Relaxation-Dispersion NMR Spectroscopy.” <i>Angewandte Chemie International Edition</i>. Wiley, 2014. <a href=\"https://doi.org/10.1002/anie.201311275\">https://doi.org/10.1002/anie.201311275</a>.","ieee":"P. Ma <i>et al.</i>, “Probing transient conformational states of proteins by solid-state R1ρ relaxation-dispersion NMR spectroscopy,” <i>Angewandte Chemie International Edition</i>, vol. 53, no. 17. Wiley, pp. 4312–4317, 2014.","short":"P. Ma, J.D. Haller, J. Zajakala, P. Macek, A.C. Sivertsen, D. Willbold, J. Boisbouvier, P. Schanda, Angewandte Chemie International Edition 53 (2014) 4312–4317.","mla":"Ma, Peixiang, et al. “Probing Transient Conformational States of Proteins by Solid-State R1ρ Relaxation-Dispersion NMR Spectroscopy.” <i>Angewandte Chemie International Edition</i>, vol. 53, no. 17, Wiley, 2014, pp. 4312–17, doi:<a href=\"https://doi.org/10.1002/anie.201311275\">10.1002/anie.201311275</a>.","ista":"Ma P, Haller JD, Zajakala J, Macek P, Sivertsen AC, Willbold D, Boisbouvier J, Schanda P. 2014. Probing transient conformational states of proteins by solid-state R1ρ relaxation-dispersion NMR spectroscopy. Angewandte Chemie International Edition. 53(17), 4312–4317."},"year":"2014","abstract":[{"text":"The function of proteins depends on their ability to sample a variety of states differing in structure and free energy. Deciphering how the various thermally accessible conformations are connected, and understanding their structures and relative energies is crucial in rationalizing protein function. Many biomolecular reactions take place within microseconds to milliseconds, and this timescale is therefore of central functional importance. Here we show that R1ρ relaxation dispersion experiments in magic‐angle‐spinning solid‐state NMR spectroscopy make it possible to investigate the thermodynamics and kinetics of such exchange process, and gain insight into structural features of short‐lived states.","lang":"eng"}],"doi":"10.1002/anie.201311275","publication_identifier":{"issn":["1433-7851"]},"day":"18"},{"volume":126,"extern":"1","year":"2014","citation":{"apa":"Stahl, E., Martin, T., Praetorius, F. M., &#38; Dietz, H. (2014). Facile and scalable preparation of pure and dense DNA origami solutions. <i>Angewandte Chemie International Edition</i>. Wiley. <a href=\"https://doi.org/10.1002/ange.201405991\">https://doi.org/10.1002/ange.201405991</a>","ama":"Stahl E, Martin T, Praetorius FM, Dietz H. Facile and scalable preparation of pure and dense DNA origami solutions. <i>Angewandte Chemie International Edition</i>. 2014;126(47):12949-12954. doi:<a href=\"https://doi.org/10.1002/ange.201405991\">10.1002/ange.201405991</a>","ieee":"E. Stahl, T. Martin, F. M. Praetorius, and H. Dietz, “Facile and scalable preparation of pure and dense DNA origami solutions,” <i>Angewandte Chemie International Edition</i>, vol. 126, no. 47. Wiley, pp. 12949–12954, 2014.","chicago":"Stahl, Evi, Thomas Martin, Florian M Praetorius, and Hendrik Dietz. “Facile and Scalable Preparation of Pure and Dense DNA Origami Solutions.” <i>Angewandte Chemie International Edition</i>. Wiley, 2014. <a href=\"https://doi.org/10.1002/ange.201405991\">https://doi.org/10.1002/ange.201405991</a>.","mla":"Stahl, Evi, et al. “Facile and Scalable Preparation of Pure and Dense DNA Origami Solutions.” <i>Angewandte Chemie International Edition</i>, vol. 126, no. 47, Wiley, 2014, pp. 12949–54, doi:<a href=\"https://doi.org/10.1002/ange.201405991\">10.1002/ange.201405991</a>.","short":"E. Stahl, T. Martin, F.M. Praetorius, H. Dietz, Angewandte Chemie International Edition 126 (2014) 12949–12954.","ista":"Stahl E, Martin T, Praetorius FM, Dietz H. 2014. Facile and scalable preparation of pure and dense DNA origami solutions. Angewandte Chemie International Edition. 126(47), 12949–12954."},"date_updated":"2023-11-07T12:14:30Z","external_id":{"pmid":["25346175"]},"day":"17","doi":"10.1002/ange.201405991","abstract":[{"lang":"eng","text":"DNA has become a prime material for assembling complex three-dimensional objects that promise utility in various areas of application. However, achieving user-defined goals with DNA objects has been hampered by the difficulty to prepare them at arbitrary concentrations and in user-defined solution conditions. Here, we describe a method that solves this problem. The method is based on poly(ethylene glycol)-induced depletion of species with high molecular weight. We demonstrate that our method is applicable to a wide spectrum of DNA shapes and that it achieves excellent recovery yields of target objects up to 97 %, while providing efficient separation from non-integrated DNA strands. DNA objects may be prepared at concentrations up to the limit of solubility, including the possibility for bringing DNA objects into a solid phase. Due to the fidelity and simplicity of our method we anticipate that it will help to catalyze the development of new types of applications that use self-assembled DNA objects."}],"quality_controlled":"1","page":"12949-12954","publisher":"Wiley","article_type":"original","scopus_import":"1","pmid":1,"_id":"14301","issue":"47","author":[{"last_name":"Stahl","first_name":"Evi","full_name":"Stahl, Evi"},{"first_name":"Thomas","last_name":"Martin","full_name":"Martin, Thomas"},{"full_name":"Praetorius, Florian M","first_name":"Florian M","last_name":"Praetorius","id":"dfec9381-4341-11ee-8fd8-faa02bba7d62"},{"full_name":"Dietz, Hendrik","first_name":"Hendrik","last_name":"Dietz"}],"article_processing_charge":"No","date_created":"2023-09-06T12:51:14Z","publication_status":"published","intvolume":"       126","title":"Facile and scalable preparation of pure and dense DNA origami solutions","main_file_link":[{"open_access":"1","url":"https://doi.org/10.1002/ange.201405991"}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","status":"public","type":"journal_article","date_published":"2014-11-17T00:00:00Z","publication_identifier":{"eissn":["1521-3773"],"issn":["1433-7851"]},"oa":1,"language":[{"iso":"eng"}],"publication":"Angewandte Chemie International Edition","oa_version":"Published Version","month":"11"},{"quality_controlled":"1","page":"10241-10244","language":[{"iso":"eng"}],"publisher":"Wiley","article_type":"letter_note","scopus_import":"1","_id":"11959","publication":"Angewandte Chemie International Edition","issue":"39","author":[{"id":"93e5e5b2-0da6-11ed-8a41-af589a024726","orcid":"0000-0001-8689-388X","full_name":"Pieber, Bartholomäus","first_name":"Bartholomäus","last_name":"Pieber"},{"full_name":"Martinez, Sabrina Teixeira","first_name":"Sabrina Teixeira","last_name":"Martinez"},{"full_name":"Cantillo, David","last_name":"Cantillo","first_name":"David"},{"last_name":"Kappe","first_name":"C. Oliver","full_name":"Kappe, C. Oliver"}],"date_created":"2022-08-24T11:01:47Z","article_processing_charge":"No","publication_status":"published","oa_version":"None","intvolume":"        52","title":"In situ generation of diimide from hydrazine and oxygen: Continuous-flow transfer hydrogenation of olefins","month":"09","volume":52,"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","status":"public","extern":"1","year":"2013","citation":{"mla":"Pieber, Bartholomäus, et al. “In Situ Generation of Diimide from Hydrazine and Oxygen: Continuous-Flow Transfer Hydrogenation of Olefins.” <i>Angewandte Chemie International Edition</i>, vol. 52, no. 39, Wiley, 2013, pp. 10241–44, doi:<a href=\"https://doi.org/10.1002/anie.201303528\">10.1002/anie.201303528</a>.","short":"B. Pieber, S.T. Martinez, D. Cantillo, C.O. Kappe, Angewandte Chemie International Edition 52 (2013) 10241–10244.","ista":"Pieber B, Martinez ST, Cantillo D, Kappe CO. 2013. In situ generation of diimide from hydrazine and oxygen: Continuous-flow transfer hydrogenation of olefins. Angewandte Chemie International Edition. 52(39), 10241–10244.","apa":"Pieber, B., Martinez, S. T., Cantillo, D., &#38; Kappe, C. O. (2013). In situ generation of diimide from hydrazine and oxygen: Continuous-flow transfer hydrogenation of olefins. <i>Angewandte Chemie International Edition</i>. Wiley. <a href=\"https://doi.org/10.1002/anie.201303528\">https://doi.org/10.1002/anie.201303528</a>","ama":"Pieber B, Martinez ST, Cantillo D, Kappe CO. In situ generation of diimide from hydrazine and oxygen: Continuous-flow transfer hydrogenation of olefins. <i>Angewandte Chemie International Edition</i>. 2013;52(39):10241-10244. doi:<a href=\"https://doi.org/10.1002/anie.201303528\">10.1002/anie.201303528</a>","chicago":"Pieber, Bartholomäus, Sabrina Teixeira Martinez, David Cantillo, and C. Oliver Kappe. “In Situ Generation of Diimide from Hydrazine and Oxygen: Continuous-Flow Transfer Hydrogenation of Olefins.” <i>Angewandte Chemie International Edition</i>. Wiley, 2013. <a href=\"https://doi.org/10.1002/anie.201303528\">https://doi.org/10.1002/anie.201303528</a>.","ieee":"B. Pieber, S. T. Martinez, D. Cantillo, and C. O. Kappe, “In situ generation of diimide from hydrazine and oxygen: Continuous-flow transfer hydrogenation of olefins,” <i>Angewandte Chemie International Edition</i>, vol. 52, no. 39. Wiley, pp. 10241–10244, 2013."},"date_updated":"2023-02-21T10:09:21Z","type":"journal_article","date_published":"2013-09-23T00:00:00Z","publication_identifier":{"eissn":["1521-3773"],"issn":["1433-7851"]},"day":"23","doi":"10.1002/anie.201303528","abstract":[{"lang":"eng","text":"No catalyst required! A highly efficient, catalyst-free process to generate diimide in situ from hydrazine monohydrate and molecular oxygen for the selective reduction of alkenes has been developed. The use of a gas–liquid segmented flow system allowed safe operating conditions and dramatically enhanced this atom-economical reaction, resulting in short processing times."}]},{"language":[{"iso":"eng"}],"quality_controlled":"1","page":"1088-1094","article_type":"letter_note","publisher":"Wiley","issue":"4","author":[{"last_name":"Kappe","first_name":"C. Oliver","full_name":"Kappe, C. Oliver"},{"id":"93e5e5b2-0da6-11ed-8a41-af589a024726","first_name":"Bartholomäus","last_name":"Pieber","orcid":"0000-0001-8689-388X","full_name":"Pieber, Bartholomäus"},{"full_name":"Dallinger, Doris","last_name":"Dallinger","first_name":"Doris"}],"scopus_import":"1","publication":"Angewandte Chemie International Edition","_id":"11960","intvolume":"        52","month":"01","title":"Microwave effects in organic synthesis: Myth or reality?","date_created":"2022-08-24T11:05:04Z","article_processing_charge":"No","oa_version":"None","publication_status":"published","status":"public","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","extern":"1","volume":52,"type":"journal_article","date_published":"2013-01-21T00:00:00Z","year":"2013","citation":{"chicago":"Kappe, C. Oliver, Bartholomäus Pieber, and Doris Dallinger. “Microwave Effects in Organic Synthesis: Myth or Reality?” <i>Angewandte Chemie International Edition</i>. Wiley, 2013. <a href=\"https://doi.org/10.1002/anie.201204103\">https://doi.org/10.1002/anie.201204103</a>.","ieee":"C. O. Kappe, B. Pieber, and D. Dallinger, “Microwave effects in organic synthesis: Myth or reality?,” <i>Angewandte Chemie International Edition</i>, vol. 52, no. 4. Wiley, pp. 1088–1094, 2013.","apa":"Kappe, C. O., Pieber, B., &#38; Dallinger, D. (2013). Microwave effects in organic synthesis: Myth or reality? <i>Angewandte Chemie International Edition</i>. Wiley. <a href=\"https://doi.org/10.1002/anie.201204103\">https://doi.org/10.1002/anie.201204103</a>","ama":"Kappe CO, Pieber B, Dallinger D. Microwave effects in organic synthesis: Myth or reality? <i>Angewandte Chemie International Edition</i>. 2013;52(4):1088-1094. doi:<a href=\"https://doi.org/10.1002/anie.201204103\">10.1002/anie.201204103</a>","ista":"Kappe CO, Pieber B, Dallinger D. 2013. Microwave effects in organic synthesis: Myth or reality? Angewandte Chemie International Edition. 52(4), 1088–1094.","short":"C.O. Kappe, B. Pieber, D. Dallinger, Angewandte Chemie International Edition 52 (2013) 1088–1094.","mla":"Kappe, C. Oliver, et al. “Microwave Effects in Organic Synthesis: Myth or Reality?” <i>Angewandte Chemie International Edition</i>, vol. 52, no. 4, Wiley, 2013, pp. 1088–94, doi:<a href=\"https://doi.org/10.1002/anie.201204103\">10.1002/anie.201204103</a>."},"date_updated":"2023-02-21T10:09:26Z","abstract":[{"lang":"eng","text":"It's not magic! The effects observed in microwave-irradiated chemical transformations can in most cases be rationalized by purely bulk thermal phenomena associated with rapid heating to elevated temperatures. As discussed in this Essay, the existence of so-called nonthermal or specific microwave effects is highly doubtful."}],"day":"21","publication_identifier":{"eissn":["1521-3773"],"issn":["1433-7851"]},"doi":"10.1002/anie.201204103"},{"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","status":"public","extern":"1","volume":51,"type":"journal_article","date_published":"2012-10-01T00:00:00Z","citation":{"ista":"Choi N-S, Chen Z, Freunberger SA, Ji X, Sun Y-K, Amine K, Yushin G, Nazar LF, Cho J, Bruce PG. 2012. Challenges facing Lithium batteries and electrical double-layer capacitors. Angewandte Chemie International Edition. 51(40), 9994–10024.","short":"N.-S. Choi, Z. Chen, S.A. Freunberger, X. Ji, Y.-K. Sun, K. Amine, G. Yushin, L.F. Nazar, J. Cho, P.G. Bruce, Angewandte Chemie International Edition 51 (2012) 9994–10024.","mla":"Choi, Nam-Soon, et al. “Challenges Facing Lithium Batteries and Electrical Double-Layer Capacitors.” <i>Angewandte Chemie International Edition</i>, vol. 51, no. 40, Wiley, 2012, pp. 9994–10024, doi:<a href=\"https://doi.org/10.1002/anie.201201429\">10.1002/anie.201201429</a>.","chicago":"Choi, Nam-Soon, Zonghai Chen, Stefan Alexander Freunberger, Xiulei Ji, Yang-Kook Sun, Khalil Amine, Gleb Yushin, Linda F. Nazar, Jaephil Cho, and Peter G. Bruce. “Challenges Facing Lithium Batteries and Electrical Double-Layer Capacitors.” <i>Angewandte Chemie International Edition</i>. Wiley, 2012. <a href=\"https://doi.org/10.1002/anie.201201429\">https://doi.org/10.1002/anie.201201429</a>.","ieee":"N.-S. Choi <i>et al.</i>, “Challenges facing Lithium batteries and electrical double-layer capacitors,” <i>Angewandte Chemie International Edition</i>, vol. 51, no. 40. Wiley, pp. 9994–10024, 2012.","ama":"Choi N-S, Chen Z, Freunberger SA, et al. Challenges facing Lithium batteries and electrical double-layer capacitors. <i>Angewandte Chemie International Edition</i>. 2012;51(40):9994-10024. doi:<a href=\"https://doi.org/10.1002/anie.201201429\">10.1002/anie.201201429</a>","apa":"Choi, N.-S., Chen, Z., Freunberger, S. A., Ji, X., Sun, Y.-K., Amine, K., … Bruce, P. G. (2012). Challenges facing Lithium batteries and electrical double-layer capacitors. <i>Angewandte Chemie International Edition</i>. Wiley. <a href=\"https://doi.org/10.1002/anie.201201429\">https://doi.org/10.1002/anie.201201429</a>"},"year":"2012","date_updated":"2021-01-12T08:12:56Z","abstract":[{"lang":"eng","text":"Energy‐storage technologies, including electrical double‐layer capacitors and rechargeable batteries, have attracted significant attention for applications in portable electronic devices, electric vehicles, bulk electricity storage at power stations, and “load leveling” of renewable sources, such as solar energy and wind power. Transforming lithium batteries and electric double‐layer capacitors requires a step change in the science underpinning these devices, including the discovery of new materials, new electrochemistry, and an increased understanding of the processes on which the devices depend. The Review will consider some of the current scientific issues underpinning lithium batteries and electric double‐layer capacitors."}],"day":"01","publication_identifier":{"issn":["1433-7851"]},"doi":"10.1002/anie.201201429","language":[{"iso":"eng"}],"quality_controlled":"1","page":"9994-10024","article_type":"original","publisher":"Wiley","issue":"40","author":[{"full_name":"Choi, Nam-Soon","last_name":"Choi","first_name":"Nam-Soon"},{"full_name":"Chen, Zonghai","first_name":"Zonghai","last_name":"Chen"},{"first_name":"Stefan Alexander","last_name":"Freunberger","orcid":"0000-0003-2902-5319","full_name":"Freunberger, Stefan Alexander","id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425"},{"full_name":"Ji, Xiulei","last_name":"Ji","first_name":"Xiulei"},{"full_name":"Sun, Yang-Kook","first_name":"Yang-Kook","last_name":"Sun"},{"first_name":"Khalil","last_name":"Amine","full_name":"Amine, Khalil"},{"full_name":"Yushin, Gleb","first_name":"Gleb","last_name":"Yushin"},{"full_name":"Nazar, Linda F.","last_name":"Nazar","first_name":"Linda F."},{"full_name":"Cho, Jaephil","last_name":"Cho","first_name":"Jaephil"},{"first_name":"Peter G.","last_name":"Bruce","full_name":"Bruce, Peter G."}],"publication":"Angewandte Chemie International Edition","_id":"7309","intvolume":"        51","title":"Challenges facing Lithium batteries and electrical double-layer capacitors","month":"10","article_processing_charge":"No","date_created":"2020-01-15T12:19:11Z","publication_status":"published","oa_version":"None"},{"publisher":"Wiley","article_type":"original","quality_controlled":"1","page":"11005-11009","language":[{"iso":"eng"}],"article_processing_charge":"No","date_created":"2020-09-18T10:09:40Z","oa_version":"None","publication_status":"published","intvolume":"        50","title":"Solid-state NMR measurements of asymmetric dipolar couplings provide insight into protein side-chain motion","month":"09","publication":"Angewandte Chemie International Edition","_id":"8464","issue":"46","author":[{"id":"7B541462-FAF6-11E9-A490-E8DFE5697425","first_name":"Paul","last_name":"Schanda","orcid":"0000-0002-9350-7606","full_name":"Schanda, Paul"},{"first_name":"Matthias","last_name":"Huber","full_name":"Huber, Matthias"},{"first_name":"Jérôme","last_name":"Boisbouvier","full_name":"Boisbouvier, Jérôme"},{"last_name":"Meier","first_name":"Beat H.","full_name":"Meier, Beat H."},{"last_name":"Ernst","first_name":"Matthias","full_name":"Ernst, Matthias"}],"volume":50,"related_material":{"link":[{"relation":"erratum","url":"https://doi.org/10.1002/anie.201206663"}]},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","status":"public","extern":"1","day":"14","publication_identifier":{"issn":["1433-7851"]},"doi":"10.1002/anie.201103944","abstract":[{"lang":"eng","text":"Nonsymmetric motion: Solid‐state NMR measurements of dipolar coupling tensors provide insight into protein dynamics. The hitherto ignored asymmetry of the dipolar coupling tensor contains valuable information about motional asymmetry, which was used in the first direct site‐resolved measurement of such tensors. Important motions such as rotamer jumps can now be directly detected in the solid state."}],"year":"2011","citation":{"mla":"Schanda, Paul, et al. “Solid-State NMR Measurements of Asymmetric Dipolar Couplings Provide Insight into Protein Side-Chain Motion.” <i>Angewandte Chemie International Edition</i>, vol. 50, no. 46, Wiley, 2011, pp. 11005–09, doi:<a href=\"https://doi.org/10.1002/anie.201103944\">10.1002/anie.201103944</a>.","short":"P. Schanda, M. Huber, J. Boisbouvier, B.H. Meier, M. Ernst, Angewandte Chemie International Edition 50 (2011) 11005–11009.","ista":"Schanda P, Huber M, Boisbouvier J, Meier BH, Ernst M. 2011. Solid-state NMR measurements of asymmetric dipolar couplings provide insight into protein side-chain motion. Angewandte Chemie International Edition. 50(46), 11005–11009.","ama":"Schanda P, Huber M, Boisbouvier J, Meier BH, Ernst M. Solid-state NMR measurements of asymmetric dipolar couplings provide insight into protein side-chain motion. <i>Angewandte Chemie International Edition</i>. 2011;50(46):11005-11009. doi:<a href=\"https://doi.org/10.1002/anie.201103944\">10.1002/anie.201103944</a>","apa":"Schanda, P., Huber, M., Boisbouvier, J., Meier, B. H., &#38; Ernst, M. (2011). Solid-state NMR measurements of asymmetric dipolar couplings provide insight into protein side-chain motion. <i>Angewandte Chemie International Edition</i>. Wiley. <a href=\"https://doi.org/10.1002/anie.201103944\">https://doi.org/10.1002/anie.201103944</a>","chicago":"Schanda, Paul, Matthias Huber, Jérôme Boisbouvier, Beat H. Meier, and Matthias Ernst. “Solid-State NMR Measurements of Asymmetric Dipolar Couplings Provide Insight into Protein Side-Chain Motion.” <i>Angewandte Chemie International Edition</i>. Wiley, 2011. <a href=\"https://doi.org/10.1002/anie.201103944\">https://doi.org/10.1002/anie.201103944</a>.","ieee":"P. Schanda, M. Huber, J. Boisbouvier, B. H. Meier, and M. Ernst, “Solid-state NMR measurements of asymmetric dipolar couplings provide insight into protein side-chain motion,” <i>Angewandte Chemie International Edition</i>, vol. 50, no. 46. Wiley, pp. 11005–11009, 2011."},"date_updated":"2021-01-12T08:19:27Z","type":"journal_article","date_published":"2011-09-14T00:00:00Z"},{"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","status":"public","extern":"1","volume":50,"type":"journal_article","date_published":"2011-09-05T00:00:00Z","year":"2011","citation":{"mla":"Freunberger, Stefan Alexander, et al. “The Lithium-Oxygen Battery with Ether-Based Electrolytes.” <i>Angewandte Chemie International Edition</i>, vol. 50, no. 37, Wiley, 2011, pp. 8609–13, doi:<a href=\"https://doi.org/10.1002/anie.201102357\">10.1002/anie.201102357</a>.","short":"S.A. Freunberger, Y. Chen, N.E. Drewett, L.J. Hardwick, F. Bardé, P.G. Bruce, Angewandte Chemie International Edition 50 (2011) 8609–8613.","ista":"Freunberger SA, Chen Y, Drewett NE, Hardwick LJ, Bardé F, Bruce PG. 2011. The Lithium-Oxygen battery with ether-based electrolytes. Angewandte Chemie International Edition. 50(37), 8609–8613.","ama":"Freunberger SA, Chen Y, Drewett NE, Hardwick LJ, Bardé F, Bruce PG. The Lithium-Oxygen battery with ether-based electrolytes. <i>Angewandte Chemie International Edition</i>. 2011;50(37):8609-8613. doi:<a href=\"https://doi.org/10.1002/anie.201102357\">10.1002/anie.201102357</a>","apa":"Freunberger, S. A., Chen, Y., Drewett, N. E., Hardwick, L. J., Bardé, F., &#38; Bruce, P. G. (2011). The Lithium-Oxygen battery with ether-based electrolytes. <i>Angewandte Chemie International Edition</i>. Wiley. <a href=\"https://doi.org/10.1002/anie.201102357\">https://doi.org/10.1002/anie.201102357</a>","ieee":"S. A. Freunberger, Y. Chen, N. E. Drewett, L. J. Hardwick, F. Bardé, and P. G. Bruce, “The Lithium-Oxygen battery with ether-based electrolytes,” <i>Angewandte Chemie International Edition</i>, vol. 50, no. 37. Wiley, pp. 8609–8613, 2011.","chicago":"Freunberger, Stefan Alexander, Yuhui Chen, Nicholas E. Drewett, Laurence J. Hardwick, Fanny Bardé, and Peter G. Bruce. “The Lithium-Oxygen Battery with Ether-Based Electrolytes.” <i>Angewandte Chemie International Edition</i>. Wiley, 2011. <a href=\"https://doi.org/10.1002/anie.201102357\">https://doi.org/10.1002/anie.201102357</a>."},"date_updated":"2021-01-12T08:12:59Z","abstract":[{"text":"The electrolyte is one of the greatest challenges facing the development of the non‐aqueous Li–O2 battery. Although ether‐based electrolytes do from Li2O2 on the first discharge, it is shown by various techniques that they also decompose and that decomposition increases while Li2O2 decreases on cycling (see picture). Thus, these electrolytes are not suitable. ","lang":"eng"}],"day":"05","publication_identifier":{"issn":["1433-7851"]},"doi":"10.1002/anie.201102357","language":[{"iso":"eng"}],"quality_controlled":"1","page":"8609-8613","article_type":"original","publisher":"Wiley","issue":"37","author":[{"orcid":"0000-0003-2902-5319","full_name":"Freunberger, Stefan Alexander","first_name":"Stefan Alexander","last_name":"Freunberger","id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425"},{"last_name":"Chen","first_name":"Yuhui","full_name":"Chen, Yuhui"},{"first_name":"Nicholas E.","last_name":"Drewett","full_name":"Drewett, Nicholas E."},{"first_name":"Laurence J.","last_name":"Hardwick","full_name":"Hardwick, Laurence J."},{"full_name":"Bardé, Fanny","last_name":"Bardé","first_name":"Fanny"},{"full_name":"Bruce, Peter G.","last_name":"Bruce","first_name":"Peter G."}],"publication":"Angewandte Chemie International Edition","_id":"7314","intvolume":"        50","title":"The Lithium-Oxygen battery with ether-based electrolytes","month":"09","date_created":"2020-01-15T12:20:19Z","article_processing_charge":"No","publication_status":"published","oa_version":"None"},{"date_updated":"2021-01-12T08:12:59Z","year":"2011","citation":{"mla":"Peng, Zhangquan, et al. “Oxygen Reactions in a Non-Aqueous Li+ Electrolyte.” <i>Angewandte Chemie International Edition</i>, vol. 50, no. 28, Wiley, 2011, pp. 6351–55, doi:<a href=\"https://doi.org/10.1002/anie.201100879\">10.1002/anie.201100879</a>.","short":"Z. Peng, S.A. Freunberger, L.J. Hardwick, Y. Chen, V. Giordani, F. Bardé, P. Novák, D. Graham, J.-M. Tarascon, P.G. Bruce, Angewandte Chemie International Edition 50 (2011) 6351–6355.","ista":"Peng Z, Freunberger SA, Hardwick LJ, Chen Y, Giordani V, Bardé F, Novák P, Graham D, Tarascon J-M, Bruce PG. 2011. Oxygen reactions in a non-aqueous Li+ electrolyte. Angewandte Chemie International Edition. 50(28), 6351–6355.","ama":"Peng Z, Freunberger SA, Hardwick LJ, et al. Oxygen reactions in a non-aqueous Li+ electrolyte. <i>Angewandte Chemie International Edition</i>. 2011;50(28):6351-6355. doi:<a href=\"https://doi.org/10.1002/anie.201100879\">10.1002/anie.201100879</a>","apa":"Peng, Z., Freunberger, S. A., Hardwick, L. J., Chen, Y., Giordani, V., Bardé, F., … Bruce, P. G. (2011). Oxygen reactions in a non-aqueous Li+ electrolyte. <i>Angewandte Chemie International Edition</i>. Wiley. <a href=\"https://doi.org/10.1002/anie.201100879\">https://doi.org/10.1002/anie.201100879</a>","chicago":"Peng, Zhangquan, Stefan Alexander Freunberger, Laurence J. Hardwick, Yuhui Chen, Vincent Giordani, Fanny Bardé, Petr Novák, Duncan Graham, Jean-Marie Tarascon, and Peter G. Bruce. “Oxygen Reactions in a Non-Aqueous Li+ Electrolyte.” <i>Angewandte Chemie International Edition</i>. Wiley, 2011. <a href=\"https://doi.org/10.1002/anie.201100879\">https://doi.org/10.1002/anie.201100879</a>.","ieee":"Z. Peng <i>et al.</i>, “Oxygen reactions in a non-aqueous Li+ electrolyte,” <i>Angewandte Chemie International Edition</i>, vol. 50, no. 28. Wiley, pp. 6351–6355, 2011."},"date_published":"2011-07-04T00:00:00Z","type":"journal_article","doi":"10.1002/anie.201100879","day":"04","publication_identifier":{"issn":["1433-7851"]},"abstract":[{"text":"Spectroscopic data (see picture) provide direct evidence that in non‐aqueous Li+ electrolyte, O2 is reduced to O2−, which then forms LiO2 on the electrode surface which disproportionates to Li2O2. On charging, Li2O2 decomposes directly, in a one‐step reaction to evolve O2 and does not pass through LiO2 as an intermediate. ","lang":"eng"}],"volume":50,"extern":"1","status":"public","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","publication":"Angewandte Chemie International Edition","_id":"7315","author":[{"full_name":"Peng, Zhangquan","last_name":"Peng","first_name":"Zhangquan"},{"id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425","last_name":"Freunberger","first_name":"Stefan Alexander","full_name":"Freunberger, Stefan Alexander","orcid":"0000-0003-2902-5319"},{"last_name":"Hardwick","first_name":"Laurence J.","full_name":"Hardwick, Laurence J."},{"full_name":"Chen, Yuhui","first_name":"Yuhui","last_name":"Chen"},{"last_name":"Giordani","first_name":"Vincent","full_name":"Giordani, Vincent"},{"full_name":"Bardé, Fanny","first_name":"Fanny","last_name":"Bardé"},{"first_name":"Petr","last_name":"Novák","full_name":"Novák, Petr"},{"last_name":"Graham","first_name":"Duncan","full_name":"Graham, Duncan"},{"last_name":"Tarascon","first_name":"Jean-Marie","full_name":"Tarascon, Jean-Marie"},{"full_name":"Bruce, Peter G.","last_name":"Bruce","first_name":"Peter G."}],"issue":"28","publication_status":"published","oa_version":"None","article_processing_charge":"No","date_created":"2020-01-15T12:20:31Z","title":"Oxygen reactions in a non-aqueous Li+ electrolyte","month":"07","intvolume":"        50","page":"6351-6355","language":[{"iso":"eng"}],"publisher":"Wiley","article_type":"original"},{"year":"2009","citation":{"ama":"Schanda P, Huber M, Verel R, Ernst M, Meier B. Direct detection of 3hJN’ hydrogen-bond scalar couplings in proteins by solid-state NMR spectroscopy. <i>Angewandte Chemie International Edition</i>. 2009;48(49):9322-9325. doi:<a href=\"https://doi.org/10.1002/anie.200904411\">10.1002/anie.200904411</a>","apa":"Schanda, P., Huber, M., Verel, R., Ernst, M., &#38; Meier, B. (2009). Direct detection of 3hJN’ hydrogen-bond scalar couplings in proteins by solid-state NMR spectroscopy. <i>Angewandte Chemie International Edition</i>. Wiley. <a href=\"https://doi.org/10.1002/anie.200904411\">https://doi.org/10.1002/anie.200904411</a>","ieee":"P. Schanda, M. Huber, R. Verel, M. Ernst, and B. Meier, “Direct detection of 3hJN’ hydrogen-bond scalar couplings in proteins by solid-state NMR spectroscopy,” <i>Angewandte Chemie International Edition</i>, vol. 48, no. 49. Wiley, pp. 9322–9325, 2009.","chicago":"Schanda, Paul, Matthias Huber, René Verel, Matthias Ernst, and Beat H. Meier. “Direct Detection of 3hJN’ Hydrogen-Bond Scalar Couplings in Proteins by Solid-State NMR Spectroscopy.” <i>Angewandte Chemie International Edition</i>. Wiley, 2009. <a href=\"https://doi.org/10.1002/anie.200904411\">https://doi.org/10.1002/anie.200904411</a>.","mla":"Schanda, Paul, et al. “Direct Detection of 3hJN’ Hydrogen-Bond Scalar Couplings in Proteins by Solid-State NMR Spectroscopy.” <i>Angewandte Chemie International Edition</i>, vol. 48, no. 49, Wiley, 2009, pp. 9322–25, doi:<a href=\"https://doi.org/10.1002/anie.200904411\">10.1002/anie.200904411</a>.","short":"P. Schanda, M. Huber, R. Verel, M. Ernst, B. Meier, Angewandte Chemie International Edition 48 (2009) 9322–9325.","ista":"Schanda P, Huber M, Verel R, Ernst M, Meier B. 2009. Direct detection of 3hJN’ hydrogen-bond scalar couplings in proteins by solid-state NMR spectroscopy. Angewandte Chemie International Edition. 48(49), 9322–9325."},"date_updated":"2021-01-12T08:19:31Z","type":"journal_article","date_published":"2009-11-17T00:00:00Z","day":"17","publication_identifier":{"issn":["1433-7851","1521-3773"]},"doi":"10.1002/anie.200904411","abstract":[{"text":"Hydrogen bonds are ubiquitous interactions in proteins, and are important for their folding and functionality. Scalar coupling constants across hydrogen bonds in the protein backbone, some as small as 0.5 Hz, can be directly measured in the solid state by NMR spectroscopy (see figure). The nuclei on both sides of the hydrogen bond can be identified and the size of the coupling constant can be measured accurately.","lang":"eng"}],"volume":48,"status":"public","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","extern":"1","_id":"8474","publication":"Angewandte Chemie International Edition","issue":"49","author":[{"id":"7B541462-FAF6-11E9-A490-E8DFE5697425","orcid":"0000-0002-9350-7606","full_name":"Schanda, Paul","first_name":"Paul","last_name":"Schanda"},{"full_name":"Huber, Matthias","first_name":"Matthias","last_name":"Huber"},{"full_name":"Verel, René","last_name":"Verel","first_name":"René"},{"last_name":"Ernst","first_name":"Matthias","full_name":"Ernst, Matthias"},{"full_name":"Meier, Beat H.","first_name":"Beat H.","last_name":"Meier"}],"date_created":"2020-09-18T10:11:33Z","article_processing_charge":"No","publication_status":"published","oa_version":"None","intvolume":"        48","month":"11","title":"Direct detection of 3hJN' hydrogen-bond scalar couplings in proteins by solid-state NMR spectroscopy","quality_controlled":"1","page":"9322-9325","keyword":["General Chemistry","Catalysis"],"language":[{"iso":"eng"}],"publisher":"Wiley","article_type":"original"},{"pmid":1,"_id":"13417","scopus_import":"1","author":[{"id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b","full_name":"Klajn, Rafal","first_name":"Rafal","last_name":"Klajn"},{"full_name":"Wesson, Paul J.","last_name":"Wesson","first_name":"Paul J."},{"first_name":"Kyle J. M.","last_name":"Bishop","full_name":"Bishop, Kyle J. M."},{"first_name":"Bartosz A.","last_name":"Grzybowski","full_name":"Grzybowski, Bartosz A."}],"issue":"38","publication_status":"published","article_processing_charge":"No","date_created":"2023-08-01T10:29:38Z","title":"Writing self-erasing images using metastable nanoparticle “inks”","intvolume":"        48","page":"7035-7039","quality_controlled":"1","publisher":"Wiley","article_type":"original","date_updated":"2023-08-08T08:59:15Z","citation":{"chicago":"Klajn, Rafal, Paul J. Wesson, Kyle J. M. Bishop, and Bartosz A. Grzybowski. “Writing Self-Erasing Images Using Metastable Nanoparticle ‘Inks.’” <i>Angewandte Chemie International Edition</i>. Wiley, 2009. <a href=\"https://doi.org/10.1002/anie.200901119\">https://doi.org/10.1002/anie.200901119</a>.","ieee":"R. Klajn, P. J. Wesson, K. J. M. Bishop, and B. A. Grzybowski, “Writing self-erasing images using metastable nanoparticle ‘inks,’” <i>Angewandte Chemie International Edition</i>, vol. 48, no. 38. Wiley, pp. 7035–7039, 2009.","ama":"Klajn R, Wesson PJ, Bishop KJM, Grzybowski BA. Writing self-erasing images using metastable nanoparticle “inks.” <i>Angewandte Chemie International Edition</i>. 2009;48(38):7035-7039. doi:<a href=\"https://doi.org/10.1002/anie.200901119\">10.1002/anie.200901119</a>","apa":"Klajn, R., Wesson, P. J., Bishop, K. J. M., &#38; Grzybowski, B. A. (2009). Writing self-erasing images using metastable nanoparticle “inks.” <i>Angewandte Chemie International Edition</i>. Wiley. <a href=\"https://doi.org/10.1002/anie.200901119\">https://doi.org/10.1002/anie.200901119</a>","ista":"Klajn R, Wesson PJ, Bishop KJM, Grzybowski BA. 2009. Writing self-erasing images using metastable nanoparticle “inks”. Angewandte Chemie International Edition. 48(38), 7035–7039.","mla":"Klajn, Rafal, et al. “Writing Self-Erasing Images Using Metastable Nanoparticle ‘Inks.’” <i>Angewandte Chemie International Edition</i>, vol. 48, no. 38, Wiley, 2009, pp. 7035–39, doi:<a href=\"https://doi.org/10.1002/anie.200901119\">10.1002/anie.200901119</a>.","short":"R. Klajn, P.J. Wesson, K.J.M. Bishop, B.A. Grzybowski, Angewandte Chemie International Edition 48 (2009) 7035–7039."},"year":"2009","external_id":{"pmid":["19533698"]},"doi":"10.1002/anie.200901119","day":"01","abstract":[{"lang":"eng","text":"Mission Impossible: Metal nanoparticles (NPs) coated with photoresponsive ligands are used as “inks” for self-erasing “paper” whereby light-induced self-assembly of the NPs is transduced into local color changes (see picture). Depending on the degree of self-assembly, multicolor images can be written using only one type of NP ink. Duration of image erasure is regulated by the surface concentration of photoactive groups and can range from seconds to days."}],"volume":48,"extern":"1","publication":"Angewandte Chemie International Edition","oa_version":"None","month":"09","language":[{"iso":"eng"}],"keyword":["General Chemistry","Catalysis"],"date_published":"2009-09-01T00:00:00Z","type":"journal_article","publication_identifier":{"eissn":["1521-3773"],"issn":["1433-7851"]},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","status":"public"},{"scopus_import":"1","pmid":1,"_id":"13421","issue":"10","author":[{"last_name":"Olson","first_name":"Mark A.","full_name":"Olson, Mark A."},{"last_name":"Braunschweig","first_name":"Adam B.","full_name":"Braunschweig, Adam B."},{"full_name":"Fang, Lei","last_name":"Fang","first_name":"Lei"},{"last_name":"Ikeda","first_name":"Taichi","full_name":"Ikeda, Taichi"},{"full_name":"Klajn, Rafal","first_name":"Rafal","last_name":"Klajn","id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b"},{"full_name":"Trabolsi, Ali","first_name":"Ali","last_name":"Trabolsi"},{"full_name":"Wesson, Paul J.","last_name":"Wesson","first_name":"Paul J."},{"full_name":"Benítez, Diego","first_name":"Diego","last_name":"Benítez"},{"first_name":"Chad A.","last_name":"Mirkin","full_name":"Mirkin, Chad A."},{"first_name":"Bartosz A.","last_name":"Grzybowski","full_name":"Grzybowski, Bartosz A."},{"full_name":"Stoddart, J. Fraser","first_name":"J. Fraser","last_name":"Stoddart"}],"date_created":"2023-08-01T10:30:30Z","article_processing_charge":"No","publication_status":"published","intvolume":"        48","title":"A bistable poly[2]catenane forms nanosuperstructures","quality_controlled":"1","page":"1792-1797","publisher":"Wiley","article_type":"original","year":"2009","citation":{"ieee":"M. A. Olson <i>et al.</i>, “A bistable poly[2]catenane forms nanosuperstructures,” <i>Angewandte Chemie International Edition</i>, vol. 48, no. 10. Wiley, pp. 1792–1797, 2009.","chicago":"Olson, Mark A., Adam B. Braunschweig, Lei Fang, Taichi Ikeda, Rafal Klajn, Ali Trabolsi, Paul J. Wesson, et al. “A Bistable Poly[2]Catenane Forms Nanosuperstructures.” <i>Angewandte Chemie International Edition</i>. Wiley, 2009. <a href=\"https://doi.org/10.1002/anie.200804558\">https://doi.org/10.1002/anie.200804558</a>.","ama":"Olson MA, Braunschweig AB, Fang L, et al. A bistable poly[2]catenane forms nanosuperstructures. <i>Angewandte Chemie International Edition</i>. 2009;48(10):1792-1797. doi:<a href=\"https://doi.org/10.1002/anie.200804558\">10.1002/anie.200804558</a>","apa":"Olson, M. A., Braunschweig, A. B., Fang, L., Ikeda, T., Klajn, R., Trabolsi, A., … Stoddart, J. F. (2009). A bistable poly[2]catenane forms nanosuperstructures. <i>Angewandte Chemie International Edition</i>. Wiley. <a href=\"https://doi.org/10.1002/anie.200804558\">https://doi.org/10.1002/anie.200804558</a>","ista":"Olson MA, Braunschweig AB, Fang L, Ikeda T, Klajn R, Trabolsi A, Wesson PJ, Benítez D, Mirkin CA, Grzybowski BA, Stoddart JF. 2009. A bistable poly[2]catenane forms nanosuperstructures. Angewandte Chemie International Edition. 48(10), 1792–1797.","mla":"Olson, Mark A., et al. “A Bistable Poly[2]Catenane Forms Nanosuperstructures.” <i>Angewandte Chemie International Edition</i>, vol. 48, no. 10, Wiley, 2009, pp. 1792–97, doi:<a href=\"https://doi.org/10.1002/anie.200804558\">10.1002/anie.200804558</a>.","short":"M.A. Olson, A.B. Braunschweig, L. Fang, T. Ikeda, R. Klajn, A. Trabolsi, P.J. Wesson, D. Benítez, C.A. Mirkin, B.A. Grzybowski, J.F. Stoddart, Angewandte Chemie International Edition 48 (2009) 1792–1797."},"date_updated":"2023-08-08T11:12:29Z","external_id":{"pmid":["19180620"]},"day":"23","doi":"10.1002/anie.200804558","abstract":[{"lang":"eng","text":"Side-chain poly[2]catenanes at the click of a switch! A bistable side-chain poly[2]catenane has been synthesized and found to form hierarchical self-assembled hollow superstructures of nanoscale dimensions in solution. Molecular electromechanical switching (see picture) of the material is demonstrated, and the ground-state equilibrium thermodynamics and switching kinetics are examined as the initial steps towards processible molecular-based electronic devices and nanoelectromechanical systems."}],"volume":48,"extern":"1","publication":"Angewandte Chemie International Edition","oa_version":"None","month":"02","keyword":["General Chemistry","Catalysis"],"language":[{"iso":"eng"}],"type":"journal_article","date_published":"2009-02-23T00:00:00Z","publication_identifier":{"eissn":["1521-3773"],"issn":["1433-7851"]},"status":"public","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87"},{"publication_identifier":{"issn":["1433-7851"],"eissn":["1521-3773"]},"type":"journal_article","date_published":"2007-11-12T00:00:00Z","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","status":"public","month":"11","oa_version":"None","publication":"Angewandte Chemie International Edition","keyword":["General Chemistry","Catalysis"],"language":[{"iso":"eng"}],"abstract":[{"text":"Changing shapes: Metastable spherical aggregates of gold nanoparticles undergo a one-to-one, thermally induced transformation into heterodimers comprising connected plate and spherical domains. By controlling the reaction time, it is possible to isolate a variety of structures differing in the relative sizes of the domains and in the overall optical properties (see picture).","lang":"eng"}],"day":"12","doi":"10.1002/anie.200702570","external_id":{"pmid":["17902083"]},"citation":{"ista":"Klajn R, Pinchuk AO, Schatz GC, Grzybowski BA. 2007. Synthesis of heterodimeric sphere–prism nanostructures via metastable gold supraspheres. Angewandte Chemie International Edition. 46(44), 8363–8367.","short":"R. Klajn, A.O. Pinchuk, G.C. Schatz, B.A. Grzybowski, Angewandte Chemie International Edition 46 (2007) 8363–8367.","mla":"Klajn, Rafal, et al. “Synthesis of Heterodimeric Sphere–Prism Nanostructures via Metastable Gold Supraspheres.” <i>Angewandte Chemie International Edition</i>, vol. 46, no. 44, Wiley, 2007, pp. 8363–67, doi:<a href=\"https://doi.org/10.1002/anie.200702570\">10.1002/anie.200702570</a>.","chicago":"Klajn, Rafal, Anatoliy O. Pinchuk, George C. Schatz, and Bartosz A. Grzybowski. “Synthesis of Heterodimeric Sphere–Prism Nanostructures via Metastable Gold Supraspheres.” <i>Angewandte Chemie International Edition</i>. Wiley, 2007. <a href=\"https://doi.org/10.1002/anie.200702570\">https://doi.org/10.1002/anie.200702570</a>.","ieee":"R. Klajn, A. O. Pinchuk, G. C. Schatz, and B. A. Grzybowski, “Synthesis of heterodimeric sphere–prism nanostructures via metastable gold supraspheres,” <i>Angewandte Chemie International Edition</i>, vol. 46, no. 44. Wiley, pp. 8363–8367, 2007.","apa":"Klajn, R., Pinchuk, A. O., Schatz, G. C., &#38; Grzybowski, B. A. (2007). Synthesis of heterodimeric sphere–prism nanostructures via metastable gold supraspheres. <i>Angewandte Chemie International Edition</i>. Wiley. <a href=\"https://doi.org/10.1002/anie.200702570\">https://doi.org/10.1002/anie.200702570</a>","ama":"Klajn R, Pinchuk AO, Schatz GC, Grzybowski BA. Synthesis of heterodimeric sphere–prism nanostructures via metastable gold supraspheres. <i>Angewandte Chemie International Edition</i>. 2007;46(44):8363-8367. doi:<a href=\"https://doi.org/10.1002/anie.200702570\">10.1002/anie.200702570</a>"},"year":"2007","date_updated":"2023-08-08T11:17:57Z","extern":"1","volume":46,"intvolume":"        46","title":"Synthesis of heterodimeric sphere–prism nanostructures via metastable gold supraspheres","article_processing_charge":"No","date_created":"2023-08-01T10:31:08Z","publication_status":"published","issue":"44","author":[{"id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b","full_name":"Klajn, Rafal","first_name":"Rafal","last_name":"Klajn"},{"first_name":"Anatoliy O.","last_name":"Pinchuk","full_name":"Pinchuk, Anatoliy O."},{"first_name":"George C.","last_name":"Schatz","full_name":"Schatz, George C."},{"full_name":"Grzybowski, Bartosz A.","last_name":"Grzybowski","first_name":"Bartosz A."}],"scopus_import":"1","_id":"13424","pmid":1,"article_type":"original","publisher":"Wiley","quality_controlled":"1","page":"8363-8367"},{"publication_identifier":{"eissn":["1521-3773"],"issn":["1433-7851"]},"type":"journal_article","date_published":"2006-08-11T00:00:00Z","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","status":"public","oa_version":"None","month":"08","publication":"Angewandte Chemie International Edition","keyword":["General Chemistry","Catalysis"],"language":[{"iso":"eng"}],"day":"11","doi":"10.1002/anie.200600881","abstract":[{"lang":"eng","text":"The fruitful core: Organic syntheses reported in the literature from 1850 to 2004 are analyzed with mathematical tools from network theory and statistical physics. There is a set of substances (the core) from which the majority of other organic compounds can be made (see picture; red: core, blue: periphery, green: islands). Search algorithms are used to identify small optimal sets of maximally useful chemicals."}],"citation":{"ista":"Bishop KJM, Klajn R, Grzybowski BA. 2006. The core and most useful molecules in organic chemistry. Angewandte Chemie International Edition. 45(32), 5348–5354.","short":"K.J.M. Bishop, R. Klajn, B.A. Grzybowski, Angewandte Chemie International Edition 45 (2006) 5348–5354.","mla":"Bishop, Kyle J. M., et al. “The Core and Most Useful Molecules in Organic Chemistry.” <i>Angewandte Chemie International Edition</i>, vol. 45, no. 32, Wiley, 2006, pp. 5348–54, doi:<a href=\"https://doi.org/10.1002/anie.200600881\">10.1002/anie.200600881</a>.","ieee":"K. J. M. Bishop, R. Klajn, and B. A. Grzybowski, “The core and most useful molecules in organic chemistry,” <i>Angewandte Chemie International Edition</i>, vol. 45, no. 32. Wiley, pp. 5348–5354, 2006.","chicago":"Bishop, Kyle J. M., Rafal Klajn, and Bartosz A. Grzybowski. “The Core and Most Useful Molecules in Organic Chemistry.” <i>Angewandte Chemie International Edition</i>. Wiley, 2006. <a href=\"https://doi.org/10.1002/anie.200600881\">https://doi.org/10.1002/anie.200600881</a>.","apa":"Bishop, K. J. M., Klajn, R., &#38; Grzybowski, B. A. (2006). The core and most useful molecules in organic chemistry. <i>Angewandte Chemie International Edition</i>. Wiley. <a href=\"https://doi.org/10.1002/anie.200600881\">https://doi.org/10.1002/anie.200600881</a>","ama":"Bishop KJM, Klajn R, Grzybowski BA. The core and most useful molecules in organic chemistry. <i>Angewandte Chemie International Edition</i>. 2006;45(32):5348-5354. doi:<a href=\"https://doi.org/10.1002/anie.200600881\">10.1002/anie.200600881</a>"},"year":"2006","date_updated":"2023-08-08T11:31:27Z","external_id":{"pmid":["16835857"]},"volume":45,"extern":"1","date_created":"2023-08-01T10:37:16Z","article_processing_charge":"No","publication_status":"published","intvolume":"        45","title":"The core and most useful molecules in organic chemistry","scopus_import":"1","pmid":1,"_id":"13429","issue":"32","author":[{"first_name":"Kyle J. M.","last_name":"Bishop","full_name":"Bishop, Kyle J. M."},{"full_name":"Klajn, Rafal","first_name":"Rafal","last_name":"Klajn","id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b"},{"full_name":"Grzybowski, Bartosz A.","first_name":"Bartosz A.","last_name":"Grzybowski"}],"publisher":"Wiley","article_type":"original","quality_controlled":"1","page":"5348-5354"}]