Effects of interaction between the chelate rings and π-conjugated systems in fused salphen complexes on UV-Vis-NIR spectra

被引:2
|
作者
Houjou, Hirohiko [1 ]
Yagi, Keisuke [1 ]
Yoshikawa, Isao [1 ]
Mutai, Toshiki [1 ]
Araki, Koji [1 ]
机构
[1] Univ Tokyo, Inst Ind Sci, Meguro Ku, 4-6-1 Komaba, Tokyo 1538505, Japan
基金
日本学术振兴会;
关键词
aromaticity; conjugation; density functional calculations; isomer effect; near-infrared absorption; polycyclic aromatic hydrocarbon; Schiff bases; transition metal; UV-Vis spectroscopy; SCHIFF-BASE COMPLEXES; SALEN COMPLEXES; NICKEL(II); POLYMERS; POLY(SALPHENYLENEETHYNYLENE)S; METALLOPOLYMERS; AROMATICITY; TAUTOMERISM; TRANSITION; OXIDATION;
D O I
10.1002/poc.3635
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Dinuclear (Zn-2, Ni-2, and NiZn) complexes of fused salphen with acene-type annelation were synthesized from 3,7-diformyl-2,6-dihydroxynaphthalene. The spectroscopic properties of these complexes were compared with those of their constitutional isomers with phene-type annelation. The acene-type complexes exhibited a characteristic absorption band in the near-infrared region that showed a noticeable solvent effect. Time-dependent density functional theory calculations suggested that the absorption arose from a pi -> pi* transition localized at the naphthalene ring, which was perturbed by the adjoining chelate rings. Effects of the connection topology in the fused salphen complexes are discussed by comparison with those of polycyclic aromatic hydrocarbons.
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页数:9
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