[{"title":"Nanoporous frameworks exhibiting multiple stimuli responsiveness","oa":1,"date_updated":"2023-08-08T07:28:10Z","article_processing_charge":"No","intvolume":"         5","scopus_import":"1","language":[{"iso":"eng"}],"publication":"Nature Communications","author":[{"full_name":"Kundu, Pintu K.","first_name":"Pintu K.","last_name":"Kundu"},{"last_name":"Olsen","first_name":"Gregory L.","full_name":"Olsen, Gregory L."},{"last_name":"Kiss","first_name":"Vladimir","full_name":"Kiss, Vladimir"},{"last_name":"Klajn","id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b","full_name":"Klajn, Rafal","first_name":"Rafal"}],"main_file_link":[{"open_access":"1","url":"https://doi.org/10.1038/ncomms4588"}],"day":"07","oa_version":"Published Version","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","publication_identifier":{"eissn":["2041-1723"]},"month":"04","pmid":1,"type":"journal_article","status":"public","citation":{"apa":"Kundu, P. K., Olsen, G. L., Kiss, V., &#38; Klajn, R. (2014). Nanoporous frameworks exhibiting multiple stimuli responsiveness. <i>Nature Communications</i>. Springer Nature. <a href=\"https://doi.org/10.1038/ncomms4588\">https://doi.org/10.1038/ncomms4588</a>","chicago":"Kundu, Pintu K., Gregory L. Olsen, Vladimir Kiss, and Rafal Klajn. “Nanoporous Frameworks Exhibiting Multiple Stimuli Responsiveness.” <i>Nature Communications</i>. Springer Nature, 2014. <a href=\"https://doi.org/10.1038/ncomms4588\">https://doi.org/10.1038/ncomms4588</a>.","ista":"Kundu PK, Olsen GL, Kiss V, Klajn R. 2014. Nanoporous frameworks exhibiting multiple stimuli responsiveness. Nature Communications. 5, 3588.","mla":"Kundu, Pintu K., et al. “Nanoporous Frameworks Exhibiting Multiple Stimuli Responsiveness.” <i>Nature Communications</i>, vol. 5, 3588, Springer Nature, 2014, doi:<a href=\"https://doi.org/10.1038/ncomms4588\">10.1038/ncomms4588</a>.","ieee":"P. K. Kundu, G. L. Olsen, V. Kiss, and R. Klajn, “Nanoporous frameworks exhibiting multiple stimuli responsiveness,” <i>Nature Communications</i>, vol. 5. Springer Nature, 2014.","ama":"Kundu PK, Olsen GL, Kiss V, Klajn R. Nanoporous frameworks exhibiting multiple stimuli responsiveness. <i>Nature Communications</i>. 2014;5. doi:<a href=\"https://doi.org/10.1038/ncomms4588\">10.1038/ncomms4588</a>","short":"P.K. Kundu, G.L. Olsen, V. Kiss, R. Klajn, Nature Communications 5 (2014)."},"date_created":"2023-08-01T09:46:27Z","keyword":["General Physics and Astronomy","General Biochemistry","Genetics and Molecular Biology","General Chemistry","Multidisciplinary"],"year":"2014","article_number":"3588","_id":"13402","article_type":"original","doi":"10.1038/ncomms4588","publication_status":"published","external_id":{"pmid":["24709950"]},"abstract":[{"text":"Nanoporous frameworks are polymeric materials built from rigid molecules, which give rise to their nanoporous structures with applications in gas sorption and storage, catalysis and others. Conceptually new applications could emerge, should these beneficial properties be manipulated by external stimuli in a reversible manner. One approach to render nanoporous frameworks responsive to external signals would be to immobilize molecular switches within their nanopores. Although the majority of molecular switches require conformational freedom to isomerize, and switching in the solid state is prohibited, the nanopores may provide enough room for the switches to efficiently isomerize. Here we describe two families of nanoporous materials incorporating the spiropyran molecular switch. These materials exhibit a variety of interesting properties, including reversible photochromism and acidochromism under solvent-free conditions, light-controlled capture and release of metal ions, as well reversible chromism induced by solvation/desolvation.","lang":"eng"}],"extern":"1","quality_controlled":"1","volume":5,"publisher":"Springer Nature","date_published":"2014-04-07T00:00:00Z"},{"language":[{"iso":"eng"}],"publication":"The Journal of Chemical Physics","issue":"6","article_processing_charge":"No","date_updated":"2023-08-22T09:01:31Z","title":"The cyclopropene radical cation: Rovibrational level structure at low energies from high-resolution photoelectron spectra","scopus_import":"1","intvolume":"       141","type":"journal_article","status":"public","pmid":1,"author":[{"last_name":"Vasilatou","full_name":"Vasilatou, K.","first_name":"K."},{"full_name":"Michaud, J. M.","first_name":"J. M.","last_name":"Michaud"},{"first_name":"Denitsa Rangelova","full_name":"Baykusheva, Denitsa Rangelova","id":"71b4d059-2a03-11ee-914d-dfa3beed6530","last_name":"Baykusheva"},{"first_name":"G.","full_name":"Grassi, G.","last_name":"Grassi"},{"full_name":"Merkt, F.","first_name":"F.","last_name":"Merkt"}],"month":"08","publication_identifier":{"eissn":["1089-7690"],"issn":["0021-9606"]},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","oa_version":"None","day":"14","article_type":"original","_id":"14019","doi":"10.1063/1.4890744","year":"2014","keyword":["Physical and Theoretical Chemistry","General Physics and Astronomy"],"date_created":"2023-08-10T06:38:30Z","citation":{"apa":"Vasilatou, K., Michaud, J. M., Baykusheva, D. R., Grassi, G., &#38; Merkt, F. (2014). The cyclopropene radical cation: Rovibrational level structure at low energies from high-resolution photoelectron spectra. <i>The Journal of Chemical Physics</i>. AIP Publishing. <a href=\"https://doi.org/10.1063/1.4890744\">https://doi.org/10.1063/1.4890744</a>","short":"K. Vasilatou, J.M. Michaud, D.R. Baykusheva, G. Grassi, F. Merkt, The Journal of Chemical Physics 141 (2014).","ama":"Vasilatou K, Michaud JM, Baykusheva DR, Grassi G, Merkt F. The cyclopropene radical cation: Rovibrational level structure at low energies from high-resolution photoelectron spectra. <i>The Journal of Chemical Physics</i>. 2014;141(6). doi:<a href=\"https://doi.org/10.1063/1.4890744\">10.1063/1.4890744</a>","ieee":"K. Vasilatou, J. M. Michaud, D. R. Baykusheva, G. Grassi, and F. Merkt, “The cyclopropene radical cation: Rovibrational level structure at low energies from high-resolution photoelectron spectra,” <i>The Journal of Chemical Physics</i>, vol. 141, no. 6. AIP Publishing, 2014.","mla":"Vasilatou, K., et al. “The Cyclopropene Radical Cation: Rovibrational Level Structure at Low Energies from High-Resolution Photoelectron Spectra.” <i>The Journal of Chemical Physics</i>, vol. 141, no. 6, 064317, AIP Publishing, 2014, doi:<a href=\"https://doi.org/10.1063/1.4890744\">10.1063/1.4890744</a>.","chicago":"Vasilatou, K., J. M. Michaud, Denitsa Rangelova Baykusheva, G. Grassi, and F. Merkt. “The Cyclopropene Radical Cation: Rovibrational Level Structure at Low Energies from High-Resolution Photoelectron Spectra.” <i>The Journal of Chemical Physics</i>. AIP Publishing, 2014. <a href=\"https://doi.org/10.1063/1.4890744\">https://doi.org/10.1063/1.4890744</a>.","ista":"Vasilatou K, Michaud JM, Baykusheva DR, Grassi G, Merkt F. 2014. The cyclopropene radical cation: Rovibrational level structure at low energies from high-resolution photoelectron spectra. The Journal of Chemical Physics. 141(6), 064317."},"article_number":"064317","date_published":"2014-08-14T00:00:00Z","publisher":"AIP Publishing","volume":141,"quality_controlled":"1","extern":"1","publication_status":"published","abstract":[{"lang":"eng","text":"The cyclopropene radical cation (c-C3H₄⁺) is an important but poorly characterized three-membered-ring hydrocarbon. We report on a measurement of the high-resolution photoelectron and photoionization spectra of cyclopropene and several deuterated isotopomers, from which we have determined the rovibrational energy level structure of the X⁺ (2)B2 ground electronic state of c-C3H₄⁺ at low energies for the first time. The synthesis of the partially deuterated isotopomers always resulted in mixtures of several isotopomers, differing in their number of D atoms and in the location of these atoms, so that the photoelectron spectra of deuterated samples are superpositions of the spectra of several isotopomers. The rotationally resolved spectra indicate a C(2v)-symmetric R0 structure for the ground electronic state of c-C3H₄⁺. Two vibrational modes of c-C3H₄⁺ are found to have vibrational wave numbers below 300 cm(-1), which is surprising for such a small cyclic hydrocarbon. The analysis of the isotopic shifts of the vibrational levels enabled the assignment of the lowest-frequency mode (fundamental wave number of ≈110 cm(-1) in c-C3H₄⁺) to the CH2 torsional mode (ν₈⁺, A2 symmetry) and of the second-lowest-frequency mode (≈210 cm(-1) in c-C3H₄⁺) to a mode combining a CH out-of-plane with a CH2 rocking motion (ν₁₅⁺, B2 symmetry). The potential energy along the CH2 torsional coordinate is flat near the equilibrium structure and leads to a pronounced anharmonicity."}],"external_id":{"pmid":["25134581"]}},{"type":"journal_article","status":"public","pmid":1,"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","main_file_link":[{"open_access":"1","url":"https://arxiv.org/abs/1311.3923"}],"day":"11","oa_version":"Preprint","month":"07","publication_identifier":{"eissn":["1079-7114"],"issn":["0031-9007"]},"arxiv":1,"author":[{"first_name":"P. M.","full_name":"Kraus, P. M.","last_name":"Kraus"},{"last_name":"Baykusheva","id":"71b4d059-2a03-11ee-914d-dfa3beed6530","full_name":"Baykusheva, Denitsa Rangelova","first_name":"Denitsa Rangelova"},{"full_name":"Wörner, H. J.","first_name":"H. J.","last_name":"Wörner"}],"publication":"Physical Review Letters","language":[{"iso":"eng"}],"scopus_import":"1","intvolume":"       113","title":"Two-pulse field-free orientation reveals anisotropy of molecular shape resonance","article_processing_charge":"No","issue":"2","oa":1,"date_updated":"2023-08-22T09:02:56Z","quality_controlled":"1","volume":113,"extern":"1","date_published":"2014-07-11T00:00:00Z","publisher":"American Physical Society","abstract":[{"lang":"eng","text":"We report the observation of macroscopic field-free orientation, i.e., more than 73% of CO molecules pointing in the same direction. This is achieved through an all-optical scheme operating at high particle densities (>10(17)  cm(-3)) that combines one-color (ω) and two-color (ω+2ω) nonresonant femtosecond laser pulses. We show that the achieved orientation solely relies on the hyperpolarizability interaction as opposed to an ionization-depletion mechanism, thus, opening a wide range of applications. The achieved strong orientation enables us to reveal the molecular-frame anisotropies of the photorecombination amplitudes and phases caused by a shape resonance. The resonance appears as a local maximum in the even-harmonic emission around 28 eV. In contrast, the odd-harmonic emission is suppressed in this spectral region through the combined effects of an asymmetric photorecombination phase and a subcycle Stark effect, generic for polar molecules, that we experimentally identify."}],"external_id":{"arxiv":["1311.3923"],"pmid":["25062172"]},"publication_status":"published","doi":"10.1103/physrevlett.113.023001","article_type":"original","_id":"14020","article_number":"023001","keyword":["General Physics and Astronomy"],"date_created":"2023-08-10T06:38:38Z","citation":{"mla":"Kraus, P. M., et al. “Two-Pulse Field-Free Orientation Reveals Anisotropy of Molecular Shape Resonance.” <i>Physical Review Letters</i>, vol. 113, no. 2, 023001, American Physical Society, 2014, doi:<a href=\"https://doi.org/10.1103/physrevlett.113.023001\">10.1103/physrevlett.113.023001</a>.","ista":"Kraus PM, Baykusheva DR, Wörner HJ. 2014. Two-pulse field-free orientation reveals anisotropy of molecular shape resonance. Physical Review Letters. 113(2), 023001.","chicago":"Kraus, P. M., Denitsa Rangelova Baykusheva, and H. J. Wörner. “Two-Pulse Field-Free Orientation Reveals Anisotropy of Molecular Shape Resonance.” <i>Physical Review Letters</i>. American Physical Society, 2014. <a href=\"https://doi.org/10.1103/physrevlett.113.023001\">https://doi.org/10.1103/physrevlett.113.023001</a>.","ama":"Kraus PM, Baykusheva DR, Wörner HJ. Two-pulse field-free orientation reveals anisotropy of molecular shape resonance. <i>Physical Review Letters</i>. 2014;113(2). doi:<a href=\"https://doi.org/10.1103/physrevlett.113.023001\">10.1103/physrevlett.113.023001</a>","ieee":"P. M. Kraus, D. R. Baykusheva, and H. J. Wörner, “Two-pulse field-free orientation reveals anisotropy of molecular shape resonance,” <i>Physical Review Letters</i>, vol. 113, no. 2. American Physical Society, 2014.","short":"P.M. Kraus, D.R. Baykusheva, H.J. Wörner, Physical Review Letters 113 (2014).","apa":"Kraus, P. M., Baykusheva, D. R., &#38; Wörner, H. J. (2014). Two-pulse field-free orientation reveals anisotropy of molecular shape resonance. <i>Physical Review Letters</i>. American Physical Society. <a href=\"https://doi.org/10.1103/physrevlett.113.023001\">https://doi.org/10.1103/physrevlett.113.023001</a>"},"year":"2014"},{"intvolume":"       111","scopus_import":"1","oa":1,"date_updated":"2021-11-29T14:05:19Z","issue":"24","article_processing_charge":"No","title":"Living clusters and crystals from low-density suspensions of active colloids","publication":"Physical Review Letters","language":[{"iso":"eng"}],"month":"12","publication_identifier":{"issn":["0031-9007"],"eissn":["1079-7114"]},"oa_version":"Preprint","main_file_link":[{"url":"https://arxiv.org/abs/1311.4681","open_access":"1"}],"day":"11","user_id":"8b945eb4-e2f2-11eb-945a-df72226e66a9","author":[{"last_name":"Mognetti","first_name":"B. M.","full_name":"Mognetti, B. M."},{"orcid":"0000-0002-7854-2139","last_name":"Šarić","id":"bf63d406-f056-11eb-b41d-f263a6566d8b","first_name":"Anđela","full_name":"Šarić, Anđela"},{"last_name":"Angioletti-Uberti","full_name":"Angioletti-Uberti, S.","first_name":"S."},{"last_name":"Cacciuto","full_name":"Cacciuto, A.","first_name":"A."},{"first_name":"C.","full_name":"Valeriani, C.","last_name":"Valeriani"},{"full_name":"Frenkel, D.","first_name":"D.","last_name":"Frenkel"}],"arxiv":1,"pmid":1,"type":"journal_article","status":"public","article_number":"245702","acknowledgement":"This work was supported by the ERC Advanced Grant 227758, the National Science Foundation under Career Grant No. DMR-0846426, the Wolfson Merit Award 2007/R3 of the Royal Society of London and the EPSRC Programme Grant EP/I001352/1. BMM acknowledge T. Curk and A. Ballard for useful discussions. C. V. acknowledges financial support from a Juan de la Cierva Fellowship, from the Marie Curie Integration Grant PCIG-GA-2011-303941 ANISOKINEQ, and from the National Project FIS2010- 16159. S. A-U acknowledges support from the Alexander von Humboldt Foundation.","year":"2013","citation":{"apa":"Mognetti, B. M., Šarić, A., Angioletti-Uberti, S., Cacciuto, A., Valeriani, C., &#38; Frenkel, D. (2013). Living clusters and crystals from low-density suspensions of active colloids. <i>Physical Review Letters</i>. American Physical Society. <a href=\"https://doi.org/10.1103/physrevlett.111.245702\">https://doi.org/10.1103/physrevlett.111.245702</a>","ama":"Mognetti BM, Šarić A, Angioletti-Uberti S, Cacciuto A, Valeriani C, Frenkel D. Living clusters and crystals from low-density suspensions of active colloids. <i>Physical Review Letters</i>. 2013;111(24). doi:<a href=\"https://doi.org/10.1103/physrevlett.111.245702\">10.1103/physrevlett.111.245702</a>","ieee":"B. M. Mognetti, A. Šarić, S. Angioletti-Uberti, A. Cacciuto, C. Valeriani, and D. Frenkel, “Living clusters and crystals from low-density suspensions of active colloids,” <i>Physical Review Letters</i>, vol. 111, no. 24. American Physical Society, 2013.","short":"B.M. Mognetti, A. Šarić, S. Angioletti-Uberti, A. Cacciuto, C. Valeriani, D. Frenkel, Physical Review Letters 111 (2013).","ista":"Mognetti BM, Šarić A, Angioletti-Uberti S, Cacciuto A, Valeriani C, Frenkel D. 2013. Living clusters and crystals from low-density suspensions of active colloids. Physical Review Letters. 111(24), 245702.","mla":"Mognetti, B. M., et al. “Living Clusters and Crystals from Low-Density Suspensions of Active Colloids.” <i>Physical Review Letters</i>, vol. 111, no. 24, 245702, American Physical Society, 2013, doi:<a href=\"https://doi.org/10.1103/physrevlett.111.245702\">10.1103/physrevlett.111.245702</a>.","chicago":"Mognetti, B. M., Anđela Šarić, S. Angioletti-Uberti, A. Cacciuto, C. Valeriani, and D. Frenkel. “Living Clusters and Crystals from Low-Density Suspensions of Active Colloids.” <i>Physical Review Letters</i>. American Physical Society, 2013. <a href=\"https://doi.org/10.1103/physrevlett.111.245702\">https://doi.org/10.1103/physrevlett.111.245702</a>."},"date_created":"2021-11-29T13:29:31Z","keyword":["general physics and astronomy"],"doi":"10.1103/physrevlett.111.245702","_id":"10384","article_type":"original","external_id":{"arxiv":["1311.4681"],"pmid":["24483677"]},"abstract":[{"lang":"eng","text":"Recent studies aimed at investigating artificial analogs of bacterial colonies have shown that low-density suspensions of self-propelled particles confined in two dimensions can assemble into finite aggregates that merge and split, but have a typical size that remains constant (living clusters). In this Letter, we address the problem of the formation of living clusters and crystals of active particles in three dimensions. We study two systems: self-propelled particles interacting via a generic attractive potential and colloids that can move toward each other as a result of active agents (e.g., by molecular motors). In both cases, fluidlike “living” clusters form. We explain this general feature in terms of the balance between active forces and regression to thermodynamic equilibrium. This balance can be quantified in terms of a dimensionless number that allows us to collapse the observed clustering behavior onto a universal curve. We also discuss how active motion affects the kinetics of crystal formation."}],"publication_status":"published","publisher":"American Physical Society","date_published":"2013-12-11T00:00:00Z","extern":"1","volume":111,"quality_controlled":"1"},{"author":[{"full_name":"Šarić, Anđela","first_name":"Anđela","last_name":"Šarić","id":"bf63d406-f056-11eb-b41d-f263a6566d8b","orcid":"0000-0002-7854-2139"},{"last_name":"Cacciuto","first_name":"Angelo","full_name":"Cacciuto, Angelo"}],"arxiv":1,"publication_identifier":{"eissn":["1079-7114"],"issn":["0031-9007"]},"month":"10","main_file_link":[{"url":"https://arxiv.org/abs/1206.3528","open_access":"1"}],"oa_version":"Preprint","day":"31","user_id":"8b945eb4-e2f2-11eb-945a-df72226e66a9","pmid":1,"type":"journal_article","status":"public","date_updated":"2021-11-29T14:29:25Z","oa":1,"article_processing_charge":"No","issue":"18","title":"Mechanism of membrane tube formation induced by adhesive nanocomponents","intvolume":"       109","scopus_import":"1","language":[{"iso":"eng"}],"publication":"Physical Review Letters","publication_status":"published","external_id":{"arxiv":["1206.3528"],"pmid":["23215334"]},"abstract":[{"lang":"eng","text":"We report numerical simulations of membrane tubulation driven by large colloidal particles. Using Monte Carlo simulations we study how the process depends on particle size and binding strength, and present accurate free energy calculations to sort out how tube formation compares with the competing budding process. We find that tube formation is a result of the collective behavior of the particles adhering on the surface, and it occurs for binding strengths that are smaller than those required for budding. We also find that long linear aggregates of particles forming on the membrane surface act as nucleation seeds for tubulation by lowering the free energy barrier associated to the process."}],"publisher":"American Physical Society","date_published":"2012-10-31T00:00:00Z","extern":"1","quality_controlled":"1","volume":109,"year":"2012","date_created":"2021-11-29T14:08:00Z","citation":{"ista":"Šarić A, Cacciuto A. 2012. Mechanism of membrane tube formation induced by adhesive nanocomponents. Physical Review Letters. 109(18), 188101.","mla":"Šarić, Anđela, and Angelo Cacciuto. “Mechanism of Membrane Tube Formation Induced by Adhesive Nanocomponents.” <i>Physical Review Letters</i>, vol. 109, no. 18, 188101, American Physical Society, 2012, doi:<a href=\"https://doi.org/10.1103/physrevlett.109.188101\">10.1103/physrevlett.109.188101</a>.","chicago":"Šarić, Anđela, and Angelo Cacciuto. “Mechanism of Membrane Tube Formation Induced by Adhesive Nanocomponents.” <i>Physical Review Letters</i>. American Physical Society, 2012. <a href=\"https://doi.org/10.1103/physrevlett.109.188101\">https://doi.org/10.1103/physrevlett.109.188101</a>.","ama":"Šarić A, Cacciuto A. Mechanism of membrane tube formation induced by adhesive nanocomponents. <i>Physical Review Letters</i>. 2012;109(18). doi:<a href=\"https://doi.org/10.1103/physrevlett.109.188101\">10.1103/physrevlett.109.188101</a>","ieee":"A. Šarić and A. Cacciuto, “Mechanism of membrane tube formation induced by adhesive nanocomponents,” <i>Physical Review Letters</i>, vol. 109, no. 18. American Physical Society, 2012.","short":"A. Šarić, A. Cacciuto, Physical Review Letters 109 (2012).","apa":"Šarić, A., &#38; Cacciuto, A. (2012). Mechanism of membrane tube formation induced by adhesive nanocomponents. <i>Physical Review Letters</i>. American Physical Society. <a href=\"https://doi.org/10.1103/physrevlett.109.188101\">https://doi.org/10.1103/physrevlett.109.188101</a>"},"keyword":["general physics and astronomy"],"article_number":"188101","_id":"10387","article_type":"original","doi":"10.1103/physrevlett.109.188101"},{"oa_version":"Preprint","day":"14","main_file_link":[{"open_access":"1","url":"https://arxiv.org/abs/1201.0036"}],"user_id":"8b945eb4-e2f2-11eb-945a-df72226e66a9","publication_identifier":{"eissn":["1079-7114"],"issn":["0031-9007"]},"month":"03","author":[{"last_name":"Šarić","id":"bf63d406-f056-11eb-b41d-f263a6566d8b","orcid":"0000-0002-7854-2139","first_name":"Anđela","full_name":"Šarić, Anđela"},{"full_name":"Cacciuto, Angelo","first_name":"Angelo","last_name":"Cacciuto"}],"arxiv":1,"pmid":1,"status":"public","type":"journal_article","intvolume":"       108","scopus_import":"1","title":"Fluid membranes can drive linear aggregation of adsorbed spherical nanoparticles","date_updated":"2021-11-29T15:12:13Z","oa":1,"issue":"11","article_processing_charge":"No","publication":"Physical Review Letters","language":[{"iso":"eng"}],"external_id":{"arxiv":["1201.0036"],"pmid":["22540513"]},"abstract":[{"text":"Using computer simulations, we show that lipid membranes can mediate linear aggregation of spherical nanoparticles binding to it for a wide range of biologically relevant bending rigidities. This result is in net contrast with the isotropic aggregation of nanoparticles on fluid interfaces or the expected clustering of isotropic insertions in biological membranes. We present a phase diagram indicating where linear aggregation is expected and compute explicitly the free-energy barriers associated with linear and isotropic aggregation. Finally, we provide simple scaling arguments to explain this phenomenology.","lang":"eng"}],"publication_status":"published","extern":"1","volume":108,"quality_controlled":"1","publisher":"American Physical Society","date_published":"2012-03-14T00:00:00Z","article_number":"118101","date_created":"2021-11-29T14:30:05Z","citation":{"apa":"Šarić, A., &#38; Cacciuto, A. (2012). Fluid membranes can drive linear aggregation of adsorbed spherical nanoparticles. <i>Physical Review Letters</i>. American Physical Society. <a href=\"https://doi.org/10.1103/physrevlett.108.118101\">https://doi.org/10.1103/physrevlett.108.118101</a>","short":"A. Šarić, A. Cacciuto, Physical Review Letters 108 (2012).","ieee":"A. Šarić and A. Cacciuto, “Fluid membranes can drive linear aggregation of adsorbed spherical nanoparticles,” <i>Physical Review Letters</i>, vol. 108, no. 11. American Physical Society, 2012.","ama":"Šarić A, Cacciuto A. Fluid membranes can drive linear aggregation of adsorbed spherical nanoparticles. <i>Physical Review Letters</i>. 2012;108(11). doi:<a href=\"https://doi.org/10.1103/physrevlett.108.118101\">10.1103/physrevlett.108.118101</a>","chicago":"Šarić, Anđela, and Angelo Cacciuto. “Fluid Membranes Can Drive Linear Aggregation of Adsorbed Spherical Nanoparticles.” <i>Physical Review Letters</i>. American Physical Society, 2012. <a href=\"https://doi.org/10.1103/physrevlett.108.118101\">https://doi.org/10.1103/physrevlett.108.118101</a>.","ista":"Šarić A, Cacciuto A. 2012. Fluid membranes can drive linear aggregation of adsorbed spherical nanoparticles. Physical Review Letters. 108(11), 118101.","mla":"Šarić, Anđela, and Angelo Cacciuto. “Fluid Membranes Can Drive Linear Aggregation of Adsorbed Spherical Nanoparticles.” <i>Physical Review Letters</i>, vol. 108, no. 11, 118101, American Physical Society, 2012, doi:<a href=\"https://doi.org/10.1103/physrevlett.108.118101\">10.1103/physrevlett.108.118101</a>."},"keyword":["general physics and astronomy"],"acknowledgement":"This work was supported by the National Science Foundation under Career Grant No. DMR-0846426.\r\n","year":"2012","doi":"10.1103/physrevlett.108.118101","article_type":"original","_id":"10388"},{"language":[{"iso":"eng"}],"publication":"Physical Chemistry Chemical Physics","title":"Quantum mechanical study of secondary structure formation in protected dipeptides","date_updated":"2021-10-12T09:49:22Z","issue":"18","article_processing_charge":"No","intvolume":"        12","pmid":1,"status":"public","type":"journal_article","author":[{"full_name":"Šarić, Anđela","first_name":"Anđela","orcid":"0000-0002-7854-2139","last_name":"Šarić","id":"bf63d406-f056-11eb-b41d-f263a6566d8b"},{"last_name":"Hrenar","first_name":"T.","full_name":"Hrenar, T."},{"last_name":"Mališ","full_name":"Mališ, M.","first_name":"M."},{"first_name":"N.","full_name":"Došlić, N.","last_name":"Došlić"}],"main_file_link":[{"url":"https://europepmc.org/article/med/20428547"}],"day":"16","oa_version":"None","user_id":"8b945eb4-e2f2-11eb-945a-df72226e66a9","publication_identifier":{"issn":["1463-9076","1463-9084"]},"month":"03","_id":"10128","article_type":"original","doi":"10.1039/b923041f","date_created":"2021-10-12T08:44:34Z","citation":{"mla":"Šarić, Anđela, et al. “Quantum Mechanical Study of Secondary Structure Formation in Protected Dipeptides.” <i>Physical Chemistry Chemical Physics</i>, vol. 12, no. 18, Royal Society of Chemistry , 2010, pp. 4678–85, doi:<a href=\"https://doi.org/10.1039/b923041f\">10.1039/b923041f</a>.","chicago":"Šarić, Anđela, T. Hrenar, M. Mališ, and N. Došlić. “Quantum Mechanical Study of Secondary Structure Formation in Protected Dipeptides.” <i>Physical Chemistry Chemical Physics</i>. Royal Society of Chemistry , 2010. <a href=\"https://doi.org/10.1039/b923041f\">https://doi.org/10.1039/b923041f</a>.","ista":"Šarić A, Hrenar T, Mališ M, Došlić N. 2010. Quantum mechanical study of secondary structure formation in protected dipeptides. Physical Chemistry Chemical Physics. 12(18), 4678–4685.","ama":"Šarić A, Hrenar T, Mališ M, Došlić N. Quantum mechanical study of secondary structure formation in protected dipeptides. <i>Physical Chemistry Chemical Physics</i>. 2010;12(18):4678-4685. doi:<a href=\"https://doi.org/10.1039/b923041f\">10.1039/b923041f</a>","ieee":"A. Šarić, T. Hrenar, M. Mališ, and N. Došlić, “Quantum mechanical study of secondary structure formation in protected dipeptides,” <i>Physical Chemistry Chemical Physics</i>, vol. 12, no. 18. Royal Society of Chemistry , pp. 4678–4685, 2010.","short":"A. Šarić, T. Hrenar, M. Mališ, N. Došlić, Physical Chemistry Chemical Physics 12 (2010) 4678–4685.","apa":"Šarić, A., Hrenar, T., Mališ, M., &#38; Došlić, N. (2010). Quantum mechanical study of secondary structure formation in protected dipeptides. <i>Physical Chemistry Chemical Physics</i>. Royal Society of Chemistry . <a href=\"https://doi.org/10.1039/b923041f\">https://doi.org/10.1039/b923041f</a>"},"keyword":["Physical and Theoretical Chemistry","General Physics and Astronomy"],"acknowledgement":"This work has been supported by the MZOŠ projects 098-0352851-2921 and 119-1191342-2959.","year":"2010","extern":"1","page":"4678-4685","volume":12,"quality_controlled":"1","publisher":"Royal Society of Chemistry ","date_published":"2010-03-16T00:00:00Z","publication_status":"published","external_id":{"pmid":["20428547"]},"abstract":[{"lang":"eng","text":"An extensive computational study of the conformational preferences of three capped dipeptides: Ac-Xxx-Phe-NH2, Xxx = Gly, Ala, Val is reported. On the basis of local second-order Møller–Plesset perturbation theory (LMP2) and DFT computations we were able to identify the experimentally observed conformers as γL–γL(g−) and β-turn I(g+) in Ac-Gly-Phe-NH2, and Ac-Ala-Phe-NH2, and as the closely related γL(g+)–γL(g−) and β-turn I(a,g+) in Ac-Val-Phe-NH2. In contrast to the experimental observation that peptides with bulky side chain have a propensity for β-turns, we show that in Ac-Val-Phe-NH2 the minimum energy structure corresponds to the experimentally non detected β-strand."}]},{"publication":"Physical Review Letters","language":[{"iso":"eng"}],"scopus_import":"1","intvolume":"       104","title":"Effective elasticity of a flexible filament bound to a deformable cylindrical surface","date_updated":"2021-11-30T08:11:19Z","oa":1,"issue":"22","article_processing_charge":"No","pmid":1,"type":"journal_article","status":"public","oa_version":"Preprint","day":"03","main_file_link":[{"open_access":"1","url":"https://arxiv.org/abs/1005.2429"}],"user_id":"8b945eb4-e2f2-11eb-945a-df72226e66a9","publication_identifier":{"issn":["0031-9007"],"eissn":["1079-7114"]},"month":"06","author":[{"last_name":"Šarić","id":"bf63d406-f056-11eb-b41d-f263a6566d8b","orcid":"0000-0002-7854-2139","first_name":"Anđela","full_name":"Šarić, Anđela"},{"full_name":"Pàmies, Josep C.","first_name":"Josep C.","last_name":"Pàmies"},{"full_name":"Cacciuto, Angelo","first_name":"Angelo","last_name":"Cacciuto"}],"arxiv":1,"doi":"10.1103/physrevlett.104.226101","article_type":"original","_id":"10391","article_number":"226101","date_created":"2021-11-29T15:14:33Z","citation":{"short":"A. Šarić, J.C. Pàmies, A. Cacciuto, Physical Review Letters 104 (2010).","ama":"Šarić A, Pàmies JC, Cacciuto A. Effective elasticity of a flexible filament bound to a deformable cylindrical surface. <i>Physical Review Letters</i>. 2010;104(22). doi:<a href=\"https://doi.org/10.1103/physrevlett.104.226101\">10.1103/physrevlett.104.226101</a>","ieee":"A. Šarić, J. C. Pàmies, and A. Cacciuto, “Effective elasticity of a flexible filament bound to a deformable cylindrical surface,” <i>Physical Review Letters</i>, vol. 104, no. 22. American Physical Society, 2010.","mla":"Šarić, Anđela, et al. “Effective Elasticity of a Flexible Filament Bound to a Deformable Cylindrical Surface.” <i>Physical Review Letters</i>, vol. 104, no. 22, 226101, American Physical Society, 2010, doi:<a href=\"https://doi.org/10.1103/physrevlett.104.226101\">10.1103/physrevlett.104.226101</a>.","ista":"Šarić A, Pàmies JC, Cacciuto A. 2010. Effective elasticity of a flexible filament bound to a deformable cylindrical surface. Physical Review Letters. 104(22), 226101.","chicago":"Šarić, Anđela, Josep C. Pàmies, and Angelo Cacciuto. “Effective Elasticity of a Flexible Filament Bound to a Deformable Cylindrical Surface.” <i>Physical Review Letters</i>. American Physical Society, 2010. <a href=\"https://doi.org/10.1103/physrevlett.104.226101\">https://doi.org/10.1103/physrevlett.104.226101</a>.","apa":"Šarić, A., Pàmies, J. C., &#38; Cacciuto, A. (2010). Effective elasticity of a flexible filament bound to a deformable cylindrical surface. <i>Physical Review Letters</i>. American Physical Society. <a href=\"https://doi.org/10.1103/physrevlett.104.226101\">https://doi.org/10.1103/physrevlett.104.226101</a>"},"keyword":["general physics and astronomy"],"acknowledgement":"This work was supported by the National Science Foundation under Career Grant No. DMR-0846426.","year":"2010","extern":"1","quality_controlled":"1","volume":104,"publisher":"American Physical Society","date_published":"2010-06-03T00:00:00Z","external_id":{"pmid":["20867183"],"arxiv":["1005.2429"]},"abstract":[{"text":"We use numerical simulations to show how a fully flexible filament binding to a deformable cylindrical surface may acquire a macroscopic persistence length and a helical conformation. This is a result of the nontrivial elastic response to deformations of elastic sheets. We find that the filament’s helical pitch is completely determined by the mechanical properties of the surface, and can be easily tuned by varying the surface stretching rigidity. We propose simple scaling arguments to understand the physical mechanism behind this phenomenon and present a phase diagram indicating under what conditions one should expect a fully flexible chain to behave as a helical semiflexible filament. Finally, we discuss the implications of our results.","lang":"eng"}],"publication_status":"published"},{"publication_identifier":{"issn":["0951-7715","1361-6544"]},"month":"06","abstract":[{"lang":"eng","text":"We introduce a new potential-theoretic definition of the dimension spectrum  of a probability measure for q > 1 and explain its relation to prior definitions. We apply this definition to prove that if  and  is a Borel probability measure with compact support in , then under almost every linear transformation from  to , the q-dimension of the image of  is ; in particular, the q-dimension of  is preserved provided . We also present results on the preservation of information dimension  and pointwise dimension. Finally, for  and q > 2 we give examples for which  is not preserved by any linear transformation into . All results for typical linear transformations are also proved for typical (in the sense of prevalence) continuously differentiable functions."}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","day":"19","oa_version":"None","author":[{"last_name":"Hunt","full_name":"Hunt, Brian R","first_name":"Brian R"},{"last_name":"Kaloshin","id":"FE553552-CDE8-11E9-B324-C0EBE5697425","orcid":"0000-0002-6051-2628","first_name":"Vadim","full_name":"Kaloshin, Vadim"}],"publication_status":"published","status":"public","date_published":"1997-06-19T00:00:00Z","type":"journal_article","publisher":"IOP Publishing","quality_controlled":"1","volume":10,"extern":"1","page":"1031-1046","intvolume":"        10","issue":"5","article_processing_charge":"No","year":"1997","date_updated":"2021-01-12T08:19:53Z","keyword":["Mathematical Physics","General Physics and Astronomy","Applied Mathematics","Statistical and Nonlinear Physics"],"citation":{"chicago":"Hunt, Brian R, and Vadim Kaloshin. “How Projections Affect the Dimension Spectrum of Fractal Measures.” <i>Nonlinearity</i>. IOP Publishing, 1997. <a href=\"https://doi.org/10.1088/0951-7715/10/5/002\">https://doi.org/10.1088/0951-7715/10/5/002</a>.","mla":"Hunt, Brian R., and Vadim Kaloshin. “How Projections Affect the Dimension Spectrum of Fractal Measures.” <i>Nonlinearity</i>, vol. 10, no. 5, IOP Publishing, 1997, pp. 1031–46, doi:<a href=\"https://doi.org/10.1088/0951-7715/10/5/002\">10.1088/0951-7715/10/5/002</a>.","ista":"Hunt BR, Kaloshin V. 1997. How projections affect the dimension spectrum of fractal measures. Nonlinearity. 10(5), 1031–1046.","short":"B.R. Hunt, V. Kaloshin, Nonlinearity 10 (1997) 1031–1046.","ama":"Hunt BR, Kaloshin V. How projections affect the dimension spectrum of fractal measures. <i>Nonlinearity</i>. 1997;10(5):1031-1046. doi:<a href=\"https://doi.org/10.1088/0951-7715/10/5/002\">10.1088/0951-7715/10/5/002</a>","ieee":"B. R. Hunt and V. Kaloshin, “How projections affect the dimension spectrum of fractal measures,” <i>Nonlinearity</i>, vol. 10, no. 5. IOP Publishing, pp. 1031–1046, 1997.","apa":"Hunt, B. R., &#38; Kaloshin, V. (1997). How projections affect the dimension spectrum of fractal measures. <i>Nonlinearity</i>. IOP Publishing. <a href=\"https://doi.org/10.1088/0951-7715/10/5/002\">https://doi.org/10.1088/0951-7715/10/5/002</a>"},"title":"How projections affect the dimension spectrum of fractal measures","date_created":"2020-09-18T10:50:41Z","publication":"Nonlinearity","doi":"10.1088/0951-7715/10/5/002","_id":"8527","article_type":"original","language":[{"iso":"eng"}]}]