Isomers in the chemistry of iron carbonyls
Author:
Publisher
Walter de Gruyter GmbH
Subject
Inorganic Chemistry
Link
https://www.degruyter.com/document/doi/10.1515/revic.2011.002/pdf
Reference40 articles.
1. The mechanisms of fluxionality of [Fe3(CO)12 –n{P(OR)3}n](R = Me, n= 0–3; R = Pri, n= 2 or 3) and the X-ray structure of [Fe3(CO)10{P(OMe)3}2]
2. An investigation of the fluxionality of [Fe3(CO)11(CNBut)] and [Fe3(CO)10(CNBut){P(OMe)3}], and the X-ray structure of [Fe3(CO)10(CNBut){P(OMe)3}]
3. Unprecedented rearrangement of a diphosphene .eta.1.eta.2-bonded to iron. Synthesis and x-ray structure of Fe4 complexes containing either a .mu.4 spiro phosphorus atom or a 1, 1, 2 trimetalla diphosphorus ligand .scharw.P:P-
4. Synthesis and Structure of an Anionic Arsenic Hydride Complex: [PPN]2[HAs{Fe(CO)4}3].cntdot.0.5THF
5. Structural and Reactivity Consequences of the Presence of Lone Pairs in Main-Group-Transition-Metal Cluster Compounds: Conversion of [HAs{Fe(CO)4}3]2- into [Fe3(CO)9{.mu.3-AsFe(CO)4}2]2-
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1. A Room‐Temperature Verwey‐type Transition in Iron Oxide, Fe 5 O 6;Angewandte Chemie International Edition;2020-01-30
2. A Room‐Temperature Verwey‐type Transition in Iron Oxide, Fe 5 O 6;Angewandte Chemie;2020-01-30
3. ChemInform Abstract: Isomers in the Chemistry of Iron Carbonyls;ChemInform;2013-09-19
4. Derivatives of Photosensitive CORM‐S1 – CO Complexes of Iron and Ruthenium with the (OC) 2 M(S–C–C–NH 2 ) 2 Fragment;European Journal of Inorganic Chemistry;2012-01-31
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