Steric control of Mg–Mg bond formation vs. N2 activation in the reduction of bulky magnesium diamide complexes
Author:
Affiliation:
1. School of Chemistry, Monash University, PO Box 23, Melbourne, VIC, 3800, Australia
2. Université de Toulouse et CNRS, INSA, UPS, UMR5215, LPCNO, 135 Avenue de Rangueil, Toulouse 31077, France
Abstract
Funder
Air Force Office of Scientific Research
Alexander von Humboldt-Stiftung
Australian Research Council
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2024/CC/D3CC05787A
Reference30 articles.
1. Stable Magnesium(I) Compounds with Mg-Mg Bonds
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3. Dimeric magnesium(I) β-diketiminates: a new class of quasi-universal reducing agent
4. Magnesium−Magnesium Bond Stabilized by a Doubly Reduced α-Diimine: Synthesis and Structure of [K(THF)3]2[LMg−MgL] (L = [(2,6-iPr2C6H3)NC(Me)]22−)
5. Mg–Mg-bonded compounds with N,N′-dipp-substituted phenanthrene-diamido and o-phenylene-diamino ligands
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