Baker, M. A. B. & Berry, R. M. An introduction to the physics of the bacterial flagellar motor: a nanoscale rotary electric motor. Contemp. Phys. 50, 617\u2013632 (2009).<\/p>\n
Article<\/a>\u00a0 Schliwa, M. Molecular Motors (Wiley, 2004).<\/p>\n Vale, R. D. & Milligan, R. A. The way things move: looking under the hood of molecular motor proteins. Science 288, 88\u201395 (2000).<\/p>\n Article<\/a>\u00a0 Brown, A. I. & Sivak, D. A. Theory of nonequilibrium free energy transduction by molecular machines. Chem. Rev. 120, 434\u2013459 (2020).<\/p>\n Article<\/a>\u00a0 Goodsell, D. S. The Machinery of Life (Copernicus, 2009).<\/p>\n Aprahamian, I. The future of molecular machines. ACS Cent. Sci. 6, 347\u2013358 (2020).<\/p>\n Article<\/a>\u00a0 Kassem, S. et al. Artificial molecular motors. Chem. Soc. Rev. 46, 2592\u20132621 (2017).<\/p>\n Article<\/a>\u00a0 Astumian, R. D. Kinetic asymmetry and directionality of nonequilibrium molecular systems. Angew. Chem. Int. Ed. 63, e202306569 (2024).<\/p>\n Article<\/a>\u00a0 Mondal, A., Toyoda, R., Costil, R. & Feringa, B. L. Chemically driven rotatory molecular machines. Angew. Chem. Int. Ed. 61, e20220663 (2022).<\/p>\n Article<\/a>\u00a0 Erbas-Cakmak, S., Leigh, D. A., McTernan, C. T. & Nussbaumer, A. L. Artificial molecular machines. Chem. Rev. 115, 10081\u201310206 (2015).<\/p>\n Article<\/a>\u00a0 Corra, S., Curcio, M., Baroncini, M., Silvi, S. & Credi, A. Photoactivated artificial molecular machines that can perform tasks. Adv. Mater. 32, 1906064 (2020).<\/p>\n Article<\/a>\u00a0 Baroncini, M., Silvi, S. & Credi, A. Photo- and redox-driven artificial molecular motors. Chem. Rev. 120, 200\u2013268 (2020).<\/p>\n Article<\/a>\u00a0 Pooler, D. R. S., Lubbe, A. S., Crespi, S. & Feringa, B. L. Designing light-driven rotary molecular motors. Chem. Sci. 12, 14964\u201314986 (2021).<\/p>\n Article<\/a>\u00a0 Oruganti, B., Wang, J. & Durbeej, B. Quantum chemical design of rotary molecular motors. Int. J. Quantum Chem. 118, e25405 (2018).<\/p>\n Article<\/a>\u00a0 Sheng, J. et al. Formylation boosts the performance of light-driven overcrowded alkene-derived rotary molecular motors. Nat. Chem. 16, 1330\u20131338 (2024).<\/p>\n Article<\/a>\u00a0 Boursalian, G. B. et al. All-photochemical rotation of molecular motors with a phosphorus stereoelement. J. Am. Chem. Soc. 142, 16868\u201316876 (2020).<\/p>\n Article<\/a>\u00a0 Roke, D., Wezenberg, S. J. & Feringa, B. L. Molecular rotary motors: unidirectional motion around double bonds. Proc. Natl Acad. Sci. USA 115, 9423\u20139431 (2018).<\/p>\n Article<\/a>\u00a0 Kistemaker, J. C. M. et al. Third-generation light-driven symmetric molecular motors. J. Am. Chem. Soc. 139, 9650\u20139661 (2017).<\/p>\n Article<\/a>\u00a0 Koumura, N., Zijlstra, R. W. J., van Delden, R. A., Harada, N. & Feringa, B. L. Light-driven monodirectional molecular rotor. Nature 401, 152\u2013155 (1999).<\/p>\n Article<\/a>\u00a0 Greb, L., Eichhofer, A. & Lehn, J.-M. Synthetic molecular motors: thermal N inversion and directional photoinduced CN bond rotation of camphorquinone imines. Angew. Chem. Int. Ed. 54, 14345\u201314348 (2015).<\/p>\n Article<\/a>\u00a0 Greb, L. & Lehn, J.-M. Light-driven molecular motors: imines as four-step or two-step unidirectional rotors. J. Am. Chem. Soc. 136, 13114\u201313117 (2014).<\/p>\n Article<\/a>\u00a0 Gerwien, A., Gnannt, F., Mayer, P. & Dube, H. Photogearing as a concept for translation of precise motions at the nanoscale. Nat. Chem. 14, 670\u2013676 (2022).<\/p>\n Article<\/a>\u00a0 Wilcken, R. et al. Complete mechanism of hemithioindigo motor rotation. J. Am. Chem. Soc. 140, 5311\u20135318 (2018).<\/p>\n Article<\/a>\u00a0 Gerwien, A., Mayer, P. & Dube, H. Photon-only molecular motor with reverse temperature-dependent efficiency. J. Am. Chem. Soc. 140, 16442\u201316445 (2018).<\/p>\n Article<\/a>\u00a0 Guentner, M. et al. Sunlight-powered kHz rotation of a hemithioindigo-based molecular motor. Nat. Commun. 6, 8406 (2015).<\/p>\n Article<\/a>\u00a0 Kuntze, K. et al. A visible-light-driven molecular motor based on barbituric acid. Chem. Sci. 14, 8458\u20138465 (2023).<\/p>\n Article<\/a>\u00a0 Filatov, M. et al. Towards the engineering of a photon-only two-stroke rotary molecular motor. Nat. Commun. 13, 6433 (2022).<\/p>\n Article<\/a>\u00a0 Pooler, D. R. S., Doellerer, D., Crespi, S. & Feringa, B. L. Controlling rotary motion of molecular motors based on oxindole. Org. Chem. Front. 9, 2084\u20132092 (2022).<\/p>\n Article<\/a>\u00a0 Perrot, A., Wang, W., Buhler, E., Moulin, E. & Giuseppone, N. Bending actuation of hydrogels through rotation of light-driven molecular motors. Angew. Chem. Int. Ed. 62, e202300263 (2023).<\/p>\n Article<\/a>\u00a0 Chen, J. et al. Artificial muscle-like function from hierarchical supramolecular assembly of photoresponsive molecular motors. Nat. Chem. 10, 132\u2013138 (2018).<\/p>\n Article<\/a>\u00a0 Foy, J. T. et al. Dual-light control of nanomachines that integrate motor and modulator subunits. Nat. Nanotechnol. 12, 540\u2013545 (2017).<\/p>\n Article<\/a>\u00a0 Li, Q. et al. Macroscopic contraction of a gel induced by the integrated motion of light-driven molecular motors. Nat. Nanotechnol. 10, 161\u2013165 (2015).<\/p>\n Article<\/a>\u00a0 Qutbuddin, Y. et al. Light-activated synthetic rotary motors in lipid membranes induce shape changes through membrane expansion. Adv. Mater. 36, 2311176 (2024).<\/p>\n Article<\/a>\u00a0 Li, Q., Tan, J. & Sun, T. Light-driven Feringa motors for precision molecular mechanotherapeutics. Trends Chem. 5, 653\u2013656 (2023).<\/p>\n Article<\/a>\u00a0 Guinart, A. et al. Synthetic molecular motor activates drug delivery from polymersomes. Proc. Natl Acad. Sci. USA 120, e2301279120 (2023).<\/p>\n Article<\/a>\u00a0 Corra, S., Curcio, M. & Credi, A. Photoactivated artificial molecular motors. JACS Au 3, 1301\u20131313 (2023).<\/p>\n Article<\/a>\u00a0 Zhang, Q., Qu, D.-H., Tian, H. & Feringa, B. L. Bottom-up: can supramolecular tools deliver responsiveness from molecular motors to macroscopic materials? Matter 3, 355\u2013370 (2020).<\/p>\n Article<\/a>\u00a0 Jerca, F. A., Jerca, V. V. & Hoogenboom, R. Advances and opportunities in the exciting world of azobenzenes. Nat. Rev. Chem. 6, 51\u201369 (2022).<\/p>\n Article<\/a>\u00a0 Asaka, T., Akai, N., Kawai, A. & Shibuya, K. Photochromism of 3-butyl-1-methyl-2-phenylazoimidazolium in room temperature ionic liquids. J. Photochem. Photobiol. A 209, 12\u201318 (2010).<\/p>\n Article<\/a>\u00a0 Borsley, S., Kreidt, E., Leigh, D. A. & Roberts, B. M. W. Autonomous fuelled directional rotation about a covalent single bond. Nature 604, 80\u201385 (2022).<\/p>\n Article<\/a>\u00a0 Greenfield, J. L. et al. Molecular Photoswitches (ed. Pianowski, Z. L.) Ch. 5 (Wiley, 2022).<\/p>\n Lin, I. J. B. & Vasam, C. S. Preparation and application of N-heterocyclic carbene complexes of Ag(I). Coord. Chem. Rev. 251, 642\u2013670 (2007).<\/p>\n Article<\/a>\u00a0 Nicoli, F. et al. Photoinduced autonomous nonequilibrium operation of a molecular shuttle by combined isomerization and proton transfer through a catalytic pathway. J. Am. Chem. Soc. 144, 10180\u201310185 (2022).<\/p>\n Article<\/a>\u00a0 Hugelshofer, C. L., Mellem, K. T. & Myers, A. G. Synthesis of quaternary \u03b1-methyl \u03b1-amino acids by asymmetric alkylation of pseudoephenamine alaninamide pivaldimine. Org. Lett. 15, 3134\u20133137 (2013).<\/p>\n Article<\/a>\u00a0 Onsager, L. Reciprocal relations in irreversible processes. Phys. Rev. 37, 405\u2013426 (1931).<\/p>\n Article<\/a>\u00a0 Astumian, R. D. Microscopic reversibility as the organizing principle of molecular machines. Nat. Nanotechnol. 7, 684\u2013688 (2012).<\/p>\n Article<\/a>\u00a0 Uhl, E., Thumser, S., Mayer, P. & Dube, H. Transmission of unidirectional molecular motor rotation to a remote biaryl axis. Angew. Chem. Int. Ed. 57, 11064\u201311068 (2018).<\/p>\n Article<\/a>\u00a0 Weingart, O., Lan, Z., Thiel, W. & Thiel, W. Chiral pathways and periodic decay in cis-azobenzene photodynamics. J. Phys. Chem. Lett. 2, 1506\u20131509 (2011).<\/p>\n Article<\/a>\u00a0 Wang, Y.-T. et al. Photoisomerization of arylazopyrazole photoswitches: stereospecific excited-state relaxation. Angew. Chem. Int. Ed. 55, 14009\u201314013 (2016).<\/p>\n Article<\/a>\u00a0 Aleotti, F. et al. Multidimensional potential energy surfaces resolved at the RASPT2 level for accurate photoinduced isomerization dynamics of azobenzene. J. Chem. Theory Comput. 15, 6813\u20136823 (2019).<\/p>\n Article<\/a>\u00a0 Nenov, A. et al. UV-light-induced vibrational coherences: the key to understand Kasha rule violation in trans-azobenzene. J. Phys. Chem. Lett. 9, 1534\u20131541 (2018).<\/p>\n Article<\/a>\u00a0 Casellas, J., Bearpark, M. J. & Reguero, M. Excited-state decay in the photoisomerization of azobenzene: a new balance between mechanisms. ChemPhysChem 17, 3068\u20133079 (2016).<\/p>\n Article<\/a>\u00a0 Moghaddam, K. G., Giudetti, G., Sipma, W. & Faraji, S. Theoretical insights into the effect of size and substitution patterns of azobenzene derivatives on the DNA G-quadruplex. Phys. Chem. Chem. Phys. 22, 26944\u201326954 (2020).<\/p>\n Article<\/a>\u00a0 Vela, S., Kr\u00fcger, C. & Corminboeuf, C. Exploring chemical space in the search for improved azoheteroarene-based photoswitches. Phys. Chem. Chem. Phys. 21, 20782\u201320790 (2019).<\/p>\n Article<\/a>\u00a0 Corra, S. et al. Kinetic and energetic insights into the dissipative non-equilibrium operation of an autonomous light-powered supramolecular pump. Nat. Nanotechnol. 17, 746\u2013751 (2022).<\/p>\n Article<\/a>\u00a0 Sangchai, T., Al Shehimy, S., Penocchio, E. & Ragazzon, G. Artificial molecular ratchets: tools enabling endergonic processes. Angew. Chem. Int. Ed. 62, e202309501 (2023).<\/p>\n Article<\/a>\u00a0 Falivene, L. et al. Towards the online computer-aided design of catalytic pockets. Nat. Chem. 11, 872\u2013879 (2019).<\/p>\n Article<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n PubMed Central<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n PubMed Central<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n PubMed Central<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n PubMed Central<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n PubMed Central<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n PubMed Central<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n PubMed Central<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n PubMed Central<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n PubMed Central<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n PubMed Central<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n PubMed Central<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n PubMed Central<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n
\n CAS<\/a>\u00a0
\n PubMed<\/a>\u00a0
\n
\n Google Scholar<\/a>\u00a0\n <\/p>\n","protected":false},"excerpt":{"rendered":"Baker, M. A. B. & Berry, R. M. An introduction to the physics of the bacterial flagellar motor:…\n","protected":false},"author":2,"featured_media":263572,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[24],"tags":[61843,33248,83912,3181,85,138270,46,138268,89432,57127,12663,370,141,138269],"class_list":{"0":"post-263571","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-physics","8":"tag-analytical-chemistry","9":"tag-biochemistry","10":"tag-chemistry-food-science","11":"tag-general","12":"tag-il","13":"tag-inorganic-chemistry","14":"tag-israel","15":"tag-molecular-machines-and-motors","16":"tag-organic-chemistry","17":"tag-photochemistry","18":"tag-physical-chemistry","19":"tag-physics","20":"tag-science","21":"tag-supramolecular-chemistry"},"_links":{"self":[{"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/posts\/263571","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/comments?post=263571"}],"version-history":[{"count":0,"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/posts\/263571\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/media\/263572"}],"wp:attachment":[{"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/media?parent=263571"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/categories?post=263571"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/tags?post=263571"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}