Azulen-1-yl diazenes substituted at C-3 with phenyl-chalcogene moieties: dye synthesis, product characterization and properties
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Chemistry
Link
http://link.springer.com/content/pdf/10.1007/s00706-011-0658-4.pdf
Reference21 articles.
1. Razus AC (2000) J Chem Soc Perkin Trans 1:981
2. Razus AC, Nitu CJ (2000) J Chem Soc Perkin Trans 1:989
3. Razus AC, Birzan L, Nae S, Razus SA, Cimpeanu V, Stanciu C (2002) Synth Commun 32:825
4. Razus AC, Birzan L, Nae S, Cristian L, Chiraleu F, Cimpeanu V (2003) Dyes Pigm 57:223
5. Razus AC, Birzan L, Nae S, Surugiu MN, Cimpeanu V (2003) J Heterocycl Chem 40:995
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1. Synthesis of azulenic compounds with a homo- or hetero-atomic double bond at position 1;Arkivoc;2018-06-09
2. On the electrochemical behavior of selanyl azulenes;Journal of Solid State Electrochemistry;2016-09-09
3. 1-Phenylselanylazulenes: synthesis and selenium atom oxidation;Monatshefte für Chemie - Chemical Monthly;2014-09-05
4. A Facile Preparation, Characteristic Properties, and Crystal Structure of {4-[(E)-2-(3-Guaiazulenyl)diazenyl]phenyl}(3-guaiazulenyl)methylium Hexafluorophosphate;Bulletin of the Chemical Society of Japan;2014-04-15
5. ChemInform Abstract: Azulen-1-yl Diazenes Substituted at C-3 with Phenyl-Chalcogene Moieties: Dye Synthesis, Product Characterization and Properties.;ChemInform;2012-02-23
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