Tweaking the conjugation effects on a pair of new triazene compounds by targeted deprotonation: a spectroscopic and theoretical overview-Reference-Cited by-同舟云学术

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Tweaking the conjugation effects on a pair of new triazene compounds by targeted deprotonation: a spectroscopic and theoretical overview

Published:2023-08-29 Issue:9 Volume:29 Page:
ISSN:1610-2940
Container-title:Journal of Molecular Modeling
language:en
Short-container-title:J Mol Model

Author:

de Castro Silva Junior Henrique,Antunes Uhil,dos Santos Aline Joana Rolina Wohlmuth Alves,Moreira Eduardo Ceretta

Publisher

Springer Science and Business Media LLC

Subject

Computational Theory and Mathematics,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Catalysis

Link

https://link.springer.com/content/pdf/10.1007/s00894-023-05685-3.pdf

Reference51 articles.

1. Griess P (1866) Ueber eine neue Klasse organischer Verbindungen, in denen Wasserstoff durch Stickstoff vertreten ist. Ann Chem Pharm 137:39–91. https://doi.org/10.1002/jlac.18661370105

2. Lee W-T, Zeller M, Lugosan A (2018) Bis(triazenide), tris(triazenide), and lantern-type of triazenide iron complexes: synthesis and structural characterization. Inorg Chim Acta 477:109–113. https://doi.org/10.1016/j.ica.2018.02.014

3. Santos AJRWA, dos Santos Hackbart HC, Giacomini GX et al (2016) Inorganic and organic structures as interleavers among [bis(1-methyl-3-(p-carboxylatephenyl)triazenide 1-oxide)Ni(II)] complexes to form supramolecular arrangements. J Mol Struct 1125:426–432. https://doi.org/10.1016/j.molstruc.2016.07.021

4. Nunes MS, Garzon LR, Rampelotto RF et al (2017) Synthesis, characterization and biological activity of a gold(I) triazenide complex against chronic myeloid leukemia cells and biofilm producing microorganisms. Braz J Pharm Sci 53. https://doi.org/10.1590/s2175-97902017000400191

5. Galli P, Moretti P, Cavalleri A et al (2023) Study of the photoreaction of new triazene derivatives in solution and in polymer binder. J Photochem Photobiol A Chem 435:114331. https://doi.org/10.1016/j.jphotochem.2022.114331

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