156972-68-8Relevant articles and documents
Engineering solid-state morphologies in carbazole-ethynylene macrocycles
Finke, Aaron D.,Gross, Dustin E.,Han, Amy,Moore, Jeffrey S.
, p. 14063 - 14070 (2011)
We present a crystallographic study that systematically investigates the effects of the n-alkyl side-chain length on the crystal packing in shape-persistent macrocycles. The solid-state packing of carbazole-ethynylene- containing macrocycles is sensitive to the alkyl-chain length. In macrocycles containing n-alkyl side chains up to nine carbons in length, face-on aromatic π interactions predominate, while the addition of one carbon leads to a completely different packing arrangement. Macrocycles with C10 or C11 chains exhibit a novel packing motif wherein the alkyl chains intercalate between macrocycles, leading in one case to continuous solvent-filled channels. When crystals of the C10 macrocycle are bathed in solvent, the included molecules exchange with the external solvent, and the alkyl chain disorder changes in response to changes in the guest volume in order to retain crystallinity. Powder X-ray diffraction data indicate that alkyl-macrocycle interactions in the longer chains "emulate" the distances typical of face-to-face π interactions, leading to deceptive indicators of π stacking.
Multi-photon properties in various condensed phases of dendritic chromophores derived from carbazole and indenoquioxaline units: Synthesis and characterization
Lin, Tzu-Chau,Chien, Wei,Dai, Shu-Wen,Lin, Hao-Wu,Liu, Yueh-Ching
, p. 140 - 150 (2019/05/01)
We have used functionalized carbazoles and indenoquonoxalines as the main building units and enthynyl groups as the π-linkages to construct two novel dendritic fluorophores and studied their degenerate multi-photon absorption properties in both the solution phase and the neat-film state within femtosecond and nanosecond regions. In our experiments, these model compounds are found to manifest strong and widely dispersed two-photon absorption as well as effective power-limiting properties against ultra-short laser pulses in the near-IR region. In addition, both chromophores exhibit medium to strong three-photon-induced fluorescence, indicating such scaffold may serve as a reference structural motif for the development of three-photon materials.