Zobrazeno 1 - 4
of 4
pro vyhledávání: '"RAJESH S. BALIGAR"'
Publikováno v:
Journal of the Serbian Chemical Society, Vol 71, Iss 12, Pp 1301-1310 (2006)
The mononucleating hydrazone ligand LH3, a condensation product of salicyloylhydrazine and (2-formylphenoxy)acetic acid, was synthesized and its coordination behavior with first row transition metal(II) ions was investigated by isolating and elucidat
Externí odkaz:
https://doaj.org/article/114afaddd0fd47e38eae858a1bfa6078
Publikováno v:
Angewandte Chemie International Edition. 48:1987-1990
All wrapped up: The reaction of a 22-membered macrocycle derived from bis(o-formylphenyl)mercury and 1,2-phenylenediamine with palladium(II) results in cleavage of the macrocycle and concomitant formation of a trimetallic complex (see picture; phenyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::774d44e37b5256153e184c933c80c385
https://doi.org/10.1002/anie.200805121
https://doi.org/10.1002/anie.200805121
Publikováno v:
Journal of the Serbian Chemical Society, Vol 71, Iss 12, Pp 1301-1310 (2006)
The mononucleating hydrazone ligand LH3, a condensation product of salicyloylhydrazine and (2-formylphenoxy)acetic acid, was synthesized and its coordination behavior with first row transition metal(II) ions was investigated by isolating and elucidat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9290c6c5c8263169a7cb157c7e7965c2
http://www.doiserbia.nb.rs/img/doi/0352-5139/2006/0352-51390612301B.pdf
http://www.doiserbia.nb.rs/img/doi/0352-5139/2006/0352-51390612301B.pdf
Synthesis and structure of new Schiff base derivatives obtained from 2-(formylphenyl)mercury bromide
Publikováno v:
IndraStra Global.
Reactions of (2-formylphenyl)mercury(II) bromide 10 with primary amines give mono-, bis- and tris-Schiff base derivatives (11-18). Structures of the synthesized compounds show the presence of five-membered intramolecular Hg center dot center dot cent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bdeb0632142c38d1c71f51503816465