Novel double dealkylation of trialkylphosphite in the presence of an acid: synthesis and characterization of a 16-electron ruthenium complex bearing P(OH) 2 (OMe) ligand-Reference-Cited by-同舟云学术

Novel double dealkylation of trialkylphosphite in the presence of an acid: synthesis and characterization of a 16-electron ruthenium complex bearing P(OH) 2 (OMe) ligand

Published:2004-05 Issue:5 Volume:7 Page:654-656
ISSN:1387-7003
Container-title:Inorganic Chemistry Communications
language:en
Short-container-title:Inorganic Chemistry Communications

Author:

Nagaraja C.M.,Nethaji Munirathinam,Jagirdar Balaji R.

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Physical and Theoretical Chemistry

Reference11 articles.

1. Arbuzov-like dealkylation reactions of transition-metal-phosphite complexes

2. Synthesis by the Arbuzov-like dealkylation reaction, characterization, and reactivity of phosphonate and amino-substituted phosphonate ruthenium complexes, [(η5-C5H5)(CO)2Ru{P(O)(OR)n(NC4H8) 2−n}] (n = 0–2), and comparison with the iron analogues

3. Demethylation of trimethylphosphite promoted by dichlorodiphosphineplatinum and palladium complexes. Structures of the metallophosphonate complexes [Pt(P∧P){P(O)(OMe)2}2] (P∧P=dppe, dppp)

4. Influence of the Cone Angles and the π-Acceptor Properties of Phosphorus-Containing Ligands in the Chemistry of Dihydrogen Complexes of Ruthenium

5. Observation of a Large Coupling of a Bound Dihydrogen Ligand to Phosphorus Ligands in trans-[(dppe)2Ru(η2-H2)(PF(OMe)2)][BF4]2 Complex

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