To what extent can a conjugation between two pairs of peri -nitro and peri -amino groups be realized through the naphthalene core?-Reference-Cited by-同舟云学术

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To what extent can a conjugation between two pairs of peri -nitro and peri -amino groups be realized through the naphthalene core?

Published:2013-05-06 Issue:6 Volume:26 Page:492-502
ISSN:0894-3230
Container-title:Journal of Physical Organic Chemistry
language:en
Short-container-title:J. Phys. Org. Chem.

Author:

Ozeryanskii Valery A.¹,Filatova Ekaterina A.¹,Pozharskii Alexander F.¹,Shevchuk Dmitrii A.¹,Sorokin Vladimir I.¹

Affiliation:

1. Department of Organic Chemistry; Southern Federal University; Zorge 7 344090 Rostov-on-Don Russian Federation

Funder

Russian Foundation for Basic Research

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/poc.3114/fullpdf

Reference43 articles.

1. Experimental and theoretical study of the structure of N,N-dimethyl-4-nitroaniline derivatives as model compounds for non-linear optical organic materials

2. Syntheses of novel 1,3-diazaazulene derivatives and their nonlinear optical characterization

3. Efficient π electrons delocalization in prospective push–pull non-linear optical chromophore 4-[N,N-dimethylamino]-4′-nitro stilbene (DANS): A vibrational spectroscopic study

4. Resonance Raman spectroscopy and DFT calculations of the protonation of 4-(2-pyridylazo)-N,N-dimethylaniline in solution and adsorbed on oxide surfaces

5. Permanent Electric Dipole of Gas-Phase p-Amino Benzoic Acid

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Dialkylamino and trialkylammonium groups in close proximity: intra- and intermolecular ways of formation, structural consequences, and properties. A case of metal-free directed ortho alkylation;New Journal of Chemistry;2022

2. Proton-induced fluorescence in modified quino[7,8-h]quinolines: dual sensing for protons and π-donors;Organic & Biomolecular Chemistry;2019

3. Aromaticity of peri- and para-Substituted Naphthalene-1-carbaldehyde. Comparison with 1-Nitronaphthalene;The Journal of Physical Chemistry A;2017-03-23

4. Substituents and Environment Influences on Aromaticity of peri- and para-Substituted Naphthalenes;The Journal of Physical Chemistry A;2014-08-11

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