Iron-Carbene Complexes

Iron-Carbene Complexes

Iron-Carbene Complexes

Iron-Carbene Complexes

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Overview

E.O. Fischer received the Nobel prize in 1973 for the investigations of complexes with a formal metal atom-carbon double bond. Among these, the Iron-Carbene species is readily available and has proved to be a versatile reagent in organic syntheses. It is rather simple to tune the electronicproperties of this Fischer Carbene and to control reactivity and stereospecificity of the reagent in, e.g.,
cyclopropanation reactions.
This first volume of the "Scripts in Inorganic and Organome-
tallic Chemistry" addresses graduate students in the fields ofcoordination compounds and organic synthesis. It covers the chemistry and structural aspects of iron-carbon com-
pounds with a iron-carbon double bond. The first part deals with the carbene moiety, the second with vinylidene ligands.


Product Details

ISBN-13: 9783540562580
Publisher: Springer Berlin Heidelberg
Publication date: 06/04/1993
Series: Scripts in Inorganic and Organometallic Chemistry , #1
Pages: 202
Product dimensions: 6.10(w) x 9.25(h) x 0.02(d)

Table of Contents

1 Carbene Complexes with the 5LFe=C Moiety.- 1.1 Cationic Carbene Complexes with One Carbene Ligand Bonded to Fe.- 1.1.1 Cationic Complexes Containing the 5L(2D)2Fe=C or the 5L(2D-2D)Fe=C Moiety.- 1.1.1.1 Complexes of the Type [5L(2D-2D)Fe=CR2]+ with No Heteroatom at the Carbene Carbon Atom.- 1.1.1.2 Complexes [5L(2D)2Fe=C(R)ER]+ and [5L(2D-2D)-Fe=C(R)ER]+ with One Heteroatom at the Carbene Carbon Atom.- 1.1.2 Cationic Complexes Containing the 5L(CO)(2D)Fe=C Moiety.- 1.1.2.1 Complexes [5L(CO)(2D)Fe=CRR/]+with No Heteroatom at the Carbene Carbon Atom.- 1.1.2.2 Cations of the Type [5L(CO)(2D)Fe=C(R)ER’] + with One Heteroatom at the Carbene Carbon Atom.- 1.1.2.3 Cationic Carbene Complexes of the Type [5L(CO)(2D)Fe=C(ER)2]+ with Two Heteroatoms at the Carbene Carbon Atom.- 1.1.3 Cationic Complexes Containing the 5L(CO)2Fe=C Moiety.- 1.1.3.1 Cationic Complexes of the Type [5L(CO)2Fe =CRR’]+ without Heteroatom at the Carbene Carbon Atom.- 1.1.3.2 Cationic Complexes of the Type [5L(CO)2Fe=C(R) ER’]+ with One Heteroatom at the Carbene Carbon Atom.- 1.1.3.3 Cationic Complexes of the Type [5L(CO)2Fe =C(ER)2]+ with Two Heteroatoms at the Carbene Carbon Atom.- 1.1.4 Cationic Carbene Complexes with Additional Isocyanide Ligands.- 1.1.4.1 Complexes of the Type [5L(CO)(RNC)Fe=C(ER)2]+.- 1.1.4.2 Complexes of the Type [5L(RNC)2Fe=C(ER)2]+.- 1.2 Neutral Carbene Complexes.- 1.2.1 Carbene Complexes of the Type 5L(CO)(X)Fe=C(R)ER and 5L(CO)(X)Fe=C(ER)2.- 1.2.2 Carbene Compounds of the Type 5L(CO)(2D)Fe=C(R)ER and 5L(2D)2Fe=C(R)ER.- 1.2.3 Complexes of the Type 5L(CO)2Fe=C(ER)2.- 1.2.4 Complexes of the Type 5L(CO)RFe=C(ER)2.- 1.2.5 Neutral 19 Electron Carbene Complexes.- 1.3 Anionic Carbene Complexes.- 1.4 Carbene Compounds with Two Carbene Ligands.- 2 Vinylidene Complexes.- 2.1 Cationic Complexes of the Type [5L(2D-2D)Fe=C=CRR’]+ or [5L(2D)2Fe=C=CRR,]+.- 2.2 Cationic Complexes of the Type [5L(CO)(2D)Fe=C=CRR’]+.- 2.3 Cationic Complexes of the Type [5L(CO)2Fe=C=CRR’]+.- 2.4 Cationic Compounds of the Type [Cp(CO)(2D)FeC(2D’)=CRR’]X, [Cp(CO)Fe(?-2D-2D’)C=CRR’]X, and [Cp(CO)2FeC(2D)=CRR’]X.
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