51545-36-9Relevant articles and documents
Spacer group-controlled luminescence and response of C 3-symmetric triphenylamine derivatives towards force stimuli
Han, Yanning,Zhang, Tong,Chen, Xinyu,Chen, Qiao,Xue, Pengchong
, p. 202 - 209 (2021/01/14)
Two C3-symmetric triphenylamine derivatives with three terminal cyano units as electron acceptors were prepared to investigate the effect of the spacer group on their photophysical properties and responses towards force. Their electronic transitions were carefully studied by electrochemistry, solvent-dependent spectroscopy and quantum chemical calculations. The results suggested that introducing a double bond between the donor and acceptor results in the longer absorption and emission wavelengths of TPAVCN owing to elevated HOMO and lowered LUMO energy levels and induces a larger excited state dipole moment because of the extended conjugated length. In polar solvents, both TPACN and TPAVCN possessed a longer emission wavelength. Theoretical calculations suggested that bathochromic shifts in emission bands could be ascribed to the large polar excited states owing to the light excitation-induced intramolecular charge transfer. Moreover, TPAVCN had a larger charge transfer length and average degree of the spatial extension of hole and electron distribution because of its longer molecular length. In crystals, TPAVCN had a longer emission wavelength relative to that of TPACN. Moreover, both compounds could reversibly change their fluorescence under force and solvent annealing stimuli, and their mechanochromic properties were regulated by spacer groups. TPACN changed its fluorescence from blue to cyan with a spectral shift of 12 nm after grinding, but a large spectral shift of 30 nm, and an obvious fluorescent color change from green to yellow were observed while grinding pristine TPAVCN solids.
HCl·DMPU-assisted one-pot and metal-free conversion of aldehydes to nitriles
Hammond, Gerald B.,Mudshinge, Sagar R.,Potnis, Chinmay S.,Xu, Bo
supporting information, p. 4161 - 4164 (2020/07/14)
We report an efficient HCl·DMPU assisted one-pot conversion of aldehydes into nitriles. The use of HCl·DMPU as both an acidic source as well as a non-nucleophilic base constitutes an environmentally mild alternative for the preparation of nitriles. Our protocol proceeds smoothly without the use of toxic reagents and metal catalysts. Diverse functionalized aromatic, aliphatic and allylic aldehydes incorporating various functional groups were successfully converted to nitriles in excellent to quantitative yields. This protocol is characterized by a broad substrate scope, mild reaction conditions, and high scalability. This journal is
Highly Interpenetrated Robust Microporous Hydrogen-Bonded Organic Framework for Gas Separation
Yang, Wei,Wang, Jiawei,Wang, Hailong,Bao, Zongbi,Zhao, John Cong-Gui,Chen, Banglin
, p. 6132 - 6137 (2017/11/07)
A hydrogen-bonded organic framework (HOF), HOF-11, has been successfully prepared by the slow diffusion of hexane into a tetrahydrofuran solution of tris(4-carboxyphenyl)amine (TCPA). HOF-11 has been characterized by single-crystal and powder X-ray diffra
