Premium
Thermo‐Solvatochromism of Merocyanine Polarity Probes – What Are the Consequences of Increasing Probe Lipophilicity through Annelation? (Eur. J. Org. Chem. 7/2008)
Author(s) -
Martins Clarissa T.,
Lima Michelle S.,
Bastos Erick L.,
El Seoud Omar A.
Publication year - 2008
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.200890012
Subject(s) - solvatochromism , chemistry , merocyanine , limiting , lipophilicity , excited state , solvent polarity , photochemistry , polarity (international relations) , solvent , annulation , computational chemistry , stereochemistry , organic chemistry , atomic physics , mechanical engineering , biochemistry , physics , photochromism , engineering , cell , catalysis
The cover picture shows the quinonoid and zwitterionic limiting formulas of the solvatochromic probe MeAMBr 2 [( E )‐2,6‐dibromo‐2‐(1‐methylacridinium‐4‐yl)ethenyl phenolate]. The solvatochromic behavior is influenced by the solvent‐dependent contributions of the two limiting formulas to the ground and excited states of the probe. Details are discussed in the article by O. A. El Seoud et al. on p. 1165 ff. The artwork for the cover picture was prepared by E. L. Bastos.