Redefining the Coordination Geometry and Reactivity of Guanidinate Complexes by Covalently Linking the Guanidinate Ligands. Synthesis and Reactivity of [RN{NH(R)}CN(CH2)2NC{NH(R)}NR]M(CH2Ph)2 (R = iPr; M = Ti, Zr)-Reference-Cited by-同舟云学术

Redefining the Coordination Geometry and Reactivity of Guanidinate Complexes by Covalently Linking the Guanidinate Ligands. Synthesis and Reactivity of [RN{NH(R)}CN(CH2)2NC{NH(R)}NR]M(CH2Ph)2 (R = iPr; M = Ti, Zr)

Published:2003-01-01 Issue:3 Volume:22 Page:387-389
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Ong Tiow-Gan¹,Yap Glenn P. A.¹,Richeson Darrin S.¹

Affiliation:

1. Department of Chemistry and the Center for Catalysis Research and Innovation, University of Ottawa, Ottawa, Ontario, Canada K1N 6N5

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om020830g

Reference25 articles.

1. The coordination chemistry of guanidines and guanidinates

2. Tetrasubstituted Guanidinate Anions as Supporting Ligands in Organoyttrium Chemistry

3. Iron guanidinate complexes and formation of a novel dinuclear iron(ii) species with a dianionic μ-η2∶η2 (biguanidinate) ligand

4. Mono- and Dianionic Guanidinate Ligands. Reactivity of [iPrNC(NiPr)2]Ta(NMe2)3 and [(iPrNH)C(NiPr)2]TaCl(NMe2)3 with Me3SiCl and ArNC (Ar = 2,6-Me2C6H4)

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