Selective Dehydrogenation of Amines with Respect to Coordination Geometry: Different Oxidation Products of Tricyano[bis(2-pyridylmethyl)amine]ferrate(II) between mer- and fac-Isomers-Reference-Cited by-同舟云学术

Selective Dehydrogenation of Amines with Respect to Coordination Geometry: Different Oxidation Products of Tricyano[bis(2-pyridylmethyl)amine]ferrate(II) between mer- and fac-Isomers

Published:2004-07-03 Issue:16 Volume:43 Page:5120-5127
ISSN:0020-1669
Container-title:Inorganic Chemistry
language:en
Short-container-title:Inorg. Chem.

Author:

Goto Masafumi¹,Koga Nobuhiro¹,Ohse Yasuhiko¹,Kudoh Yuka¹,Kukihara Michiko¹,Okuno Yoshinori¹,Kurosaki Hiromasa¹

Affiliation:

1. Graduate School of Pharmaceutical Sciences, Kumamoto University, Oe-honmachi 5-1, Kumamoto, 862-0973, Japan

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ic035289a

Reference35 articles.

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3. Synthesis, structural characterization, and properties of the [Mo2O2S9]2- thio anion and the [Mo4O4S18]2-, [Mo2O2S8(SCH3)]-, and [Mo2O2S8Cl]- derivatives

4. Stoichiometry and kinetics of base-promoted disproportionation with concomitant ligand oxidation of tetracyano(1,2-diamine)ferrate(III)

5. The Oxidation Products of Tetracyanoferrate(II) Chelates with Optically Active 1,2-Diamines: Tetracyano(1,2-diamine)ferrate(III)s and Tetracyano(1,2-diimine)ferrate(II)s

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