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Heterocycles as donor and acceptor units in push–pull conjugated molecules. Part 1
Author(s) -
Bradamante Silva,
Facchetti Antonio,
Pagani Giorgio A.
Publication year - 1997
Publication title -
journal of physical organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.325
H-Index - 66
eISSN - 1099-1395
pISSN - 0894-3230
DOI - 10.1002/(sici)1099-1395(199707)10:7<514::aid-poc897>3.0.co;2-j
Subject(s) - chemistry , moiety , pyrazine , pyridinium , intramolecular force , pyridine , pyridazine , ring (chemistry) , azine , thiophene , cyanine , pyrrole , conjugated system , solvatochromism , acceptor , molecule , photochemistry , indolizine , stereochemistry , medicinal chemistry , organic chemistry , fluorescence , physics , quantum mechanics , condensed matter physics , polymer
The synthesis and spectroscopic investigation of a number of push–pull ethenes in which the donor moiety is represented by a π‐excessive five‐membered heterocycle (pyrrole, indole and thiophene) and the acceptor group is a π‐deficient heterocyclic azine ring (pyridine, pyrazine, pyrimidine, pyridazine) are described. The intramolecular charge transfer in both the neutral compounds and the corresponding N ‐alkylpyridinium triflates is discussed and confirmed on the basis of three different descriptors, Δλ Het Ph ,Δλ + n , and Δλ solv1 solv2 , that take into account the substitution of a phenyl with a heterocyclic donor ring, charge effects and solvatochromism, respectively. According to the Δλ Het Ph descriptor, the intramolecular charge transfer in the described diheteroarylethenes increases upon increasing the electron‐withdrawing capacity of the acceptor, sustained by the presence of either more than one nitrogen atom or the positive charge in the heterocyclic azine. The described pyridinium derivatives belong to the rarely investigated class of dimethine cyanine dyes. The response of the 13 C and 15 N NMR chemical shift data appears to be less clear because of the low sensitivity of the NMR probes to remote substitution. © 1997 John Wiley & Sons, Ltd.