Reversible C–C Bond Formation, Halide Abstraction, and Electromers in Complexes of Iron Containing Redox-Noninnocent Pyridine-imine Ligands-Reference-Cited by-同舟云学术

Reversible C–C Bond Formation, Halide Abstraction, and Electromers in Complexes of Iron Containing Redox-Noninnocent Pyridine-imine Ligands

Published:2021-12-10 Issue:24 Volume:60 Page:18662-18673
ISSN:0020-1669
Container-title:Inorganic Chemistry
language:en
Short-container-title:Inorg. Chem.

Author:

Pokhriyal Devika¹,Heins Spencer P.¹,Sifri Renee J.¹,Gentekos Dillon T.¹,Coleman Rachael E.¹^ORCID,Wolczanski Peter T.¹^ORCID,Cundari Thomas R.²^ORCID,Fors Brett P.¹,Lancaster Kyle M.¹^ORCID,MacMillan Samantha N.¹^ORCID

Affiliation:

1. Department of Chemistry & Chemical Biology, Baker Laboratory, Cornell University, Ithaca, New York, 14853, United States

2. Department of Chemistry, CASCaM, University of North Texas, Denton, Texas 76201, United States

Funder

Division of Chemistry

Cornell University

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.inorgchem.1c01815

Reference69 articles.

1. Carbon–Carbon Bond Formation from Azaallyl and Imine Couplings about Metal–Metal Bonds

2. C–C Bond Formation and Related Reactions at the CNC Backbone in (smif)FeX (smif = 1,3-Di-(2-pyridyl)-2-azaallyl): Dimerizations, 3 + 2 Cyclization, and Nucleophilic Attack; Transfer Hydrogenations and Alkyne Trimerization (X = N(TMS)2, dpma = (Di-(2-pyridyl-methyl)-amide))

3. Synthetic Approaches to (smif)2Ti (smif = 1,3-di-(2-pyridyl)-2-azaallyl) Reveal Redox Non-Innocence and C–C Bond-Formation

4. Iron and Chromium Complexes Containing Tridentate Chelates Based on Nacnac and Imino- and Methyl-Pyridine Components: Triggering C—X Bond Formation

5. Syntheses and characterizations of α-iminopyridine compounds (alkylNCHpy)2Fe(L/Xn), and an assessment of redox non-innocence

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