Literature DB >> 17625956

Intramolecular charge transfer effects on 4-hydroxy-3-methoxybenzaldehyde.

N Rajendiran1, T Balasubramanian.   

Abstract

The absorption and fluorescence spectral characteristics of 4-hydroxy-3-methoxybenzaldehyde (HMB) have been studied in different solvents, pH and beta-cyclodextrin (beta-CD) and compared with 4-hydroxy-3,5-dimethoxybenzaldehyde (HDMB). The inclusion complex of HMB with beta-CD is analysed by UV-vis, fluorimetry, FT-IR, (1)H NMR, SEM and AM1 methods. In HMB, the normal emission (B band) is originates from a locally excited state and the longer emission (A band) is due to intramolecular charge transfer state (ICT). The OH group of HMB is present in the interior part of the beta-CD cavity and aldehyde group present in the upper part of the beta-CD cavity.

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Year:  2007        PMID: 17625956     DOI: 10.1016/j.saa.2007.04.035

Source DB:  PubMed          Journal:  Spectrochim Acta A Mol Biomol Spectrosc        ISSN: 1386-1425            Impact factor:   4.098


  4 in total

1.  Azonium-ammonium tautomerism and inclusion complexation of 1-(2,4-diamino phenylazo) naphthalene and 4-aminoazobenzene.

Authors:  G Venkatesh; A Antony Muthu Prabhu; N Rajendiran
Journal:  J Fluoresc       Date:  2011-02-01       Impact factor: 2.217

2.  Inclusion complexation of phenoxyaliphatic acid derivatives of 3,3'-bis(indolyl)methanes with β-cyclodextrin.

Authors:  A Antony Muthu Prabhu; G S Suresh Kumar
Journal:  J Fluoresc       Date:  2014-03-13       Impact factor: 2.217

3.  Intramolecular proton transfer effects on 2,6-diaminopyridine.

Authors:  A Antony Muthu Prabhu; S Siva; R K Sankaranarayanan; N Rajendiran
Journal:  J Fluoresc       Date:  2009-08-08       Impact factor: 2.217

4.  Spectral and molecular modeling studies on hydroxybenzaldehydes with native and modified cyclodextrins.

Authors:  M Jude Jenita; T Mohandass; N Rajendiran
Journal:  J Fluoresc       Date:  2013-12-06       Impact factor: 2.217

  4 in total

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