JOURNAL ARTICLE

(η3+ -Benzyl)(η4 -cyclooctadien)rhodium(I)-Komplexe / (η3 -Benzyl)(η4 -cyclooctadiene)rhodium(I) Complexes

Hans‐Otto StühlerJoachim Pickardt

Year: 1981 Journal:   Zeitschrift für Naturforschung B Vol: 36 (3)Pages: 315-321   Publisher: De Gruyter

Abstract

Abstract Reactions of [(COD)RhCl] 2 (2) (COD = 1,5-cyclooctadiene) with i-C 3 H 7 MgBr in ether and styrene or o-methylstyrene lead to formation of the complexes [(COD)Rh(η 3 -7-methyl-benzyl)] (3) and [(COD)Rh(η 3 -6,7-dimethylbenzyl)] (4), respectively. 4 was characterized by X-ray analysis. With β-methylstyrene or allylbenzene [(COD)Rh(η 3 -7-ethylbenzyl)] (5) is formed; the latter case leads to precedent isomerisation of allylbenzene to β-methyl-styrene. On the other hand no η 3 -benzylrhodium complexes could be isolated by reactions of 2 with a-methylstyrene, 2,4-dimethylstyrene, 2,6-dimethylstyrene or 2,4,6-trimethyl-styrene. The steric reasons for this behaviour are discussed.

Keywords:
Rhodium Chemistry Styrene Isomerization Cyclooctadiene Steric effects Medicinal chemistry Ether 1,5-Cyclooctadiene Organic chemistry Catalysis Copolymer

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Topics

Organometallic Complex Synthesis and Catalysis
Physical Sciences →  Chemistry →  Organic Chemistry
Asymmetric Hydrogenation and Catalysis
Physical Sciences →  Chemistry →  Inorganic Chemistry
Synthetic Organic Chemistry Methods
Physical Sciences →  Chemistry →  Organic Chemistry

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