Theoretical studies of π-loading and structural diversity in Cp3MX (M=Zr, Hf; X=H, CH3, OR, NR2) compounds
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Physical and Theoretical Chemistry
Reference86 articles.
1. The f-orbital to carbonyl 2.pi. back-bonding: the electronic structures of (.eta.5-C5H5)3UCO and (.eta.5-C5H5)3UOC
2. Bonding in tris(.eta.5-cyclopentadienyl) actinide complexes. 2. The ground electronic configurations of "base-free" Cp3An complexes (An = thorium, protactinium, uranium, neptunium, plutonium)
3. Bonding of tris(.eta.5-cyclopentadienyl)-actinide complexes. 3. Interaction of .pi.-neutral, .pi.-acidic, and .pi.-basic ligands with (.eta.5-C5H5)3U
4. The bonding in tris(η5-cyclopentadienyl) actinide complexes IV: Electronic structural effects in AnCl3 and (η5-C5H5)3An (An ≡ Th — Cf) complexes
5. Bonding in tris(.eta.5-cyclopentadienyl) actinide complexes. 5. A comparison of the bonding in neptunium, plutonium, and transplutonium compounds with that in lanthanide compounds and a transition-metal analog
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