Solid-state thermo- and photochromism in N,N′-bis(5-X-salicylidene) diamines (X = H, Br)Safin, Damir;Robeyns, Koen;Garcia, Yann(2012) RSC Advances — Vol. 2, n° 30, p. 11379-11388 (2012)
FilesRSCAdv2012.pdf Restricted Access Adobe PDF1.51 MBRequest a copyDetailsAuthorsSafin, DamirUCLouvainAuthorRobeyns, KoenUCLouvainAuthorGarcia, YannUCLouvainAuthorAbstractSixteen N,N′-bis(salicylidene)diamines of common formula (o-OHC 6H 4CN-) 2Z [Z = o-C 6H 4 (1a), m-C 6H 4 (2a), p-C 6H 4 (3a), O (4a), CH 2(p-C 6H 4) 2 (5a), O(p-C 6H 4) 2 (6a), S(p-C 6H 4) 2 (7a), SO 2(p-C 6H 4) 2 (8a)] and N,N′-bis(5-bromosalicylidene)diamines of common formula (2-OH-(5-Br)C 6H 3CN-) 2Z [Z = o-C 6H 4 (1b), m-C 6H 4 (2b), p-C 6H 4 (3), O (4b), CH 2(p-C 6H 4) 2 (5b), O(p-C 6H 4) 2 (6b), S(p-C 6H 4) 2 (7b), SO 2(p-C 6H 4) 2 (8b)] have been synthesized and characterized by elemental analysis, X-ray powder diffraction, NMR, diffuse reflectance, Raman, IR and fluorescence spectroscopy. Molecular structures of 2a, 6a, 7a, 8a and 4b were elucidated by single crystal X-ray diffraction. Their structures are stabilized by two intramolecular hydrogen bonds and weak intermolecular π⋯π stacking interactions. All molecules are thermochromic, while molecules 2a and 2b exclusively display photochromism upon irradiation at 450 and 365 nm, respectively, which is reversible and exhibits relatively slow thermal relaxation. © 2012 The Royal Society of Chemistry.Show moreAffiliationsUCLouvainSST/IMCN/MOST - Molecular Chemistry, Materials and CatalysisShow moreCitations APA Chicago FWB Safin, D., Robeyns, K., & Garcia, Y. (2012). Solid-state thermo- and photochromism in N,N′-bis(5-X-salicylidene) diamines (X = H, Br). RSC Advances, 2(30), 11379-11388. https://doi.org/10.1039/c2ra21631k (Original work published 2012)