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Reactions of 1,8-Diheterocyclotetradeca-4,11-diynes with (η4-Cycloocta-1,5-diene)(η5-cyclopentadienyl)cobalt
✍ Scribed by Volker Wolfart; Matthias Ramming; Rolf Gleiter; Bernhard Nuber; Hans Pritzkow; Frank Rominger
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 276 KB
- Volume
- 1999
- Category
- Article
- ISSN
- 1434-1948
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✦ Synopsis
The following monocyclic and bicyclic 14-membered diynes all cases we obtained an intramolecular cyclobutadiene complex stabilized with a CpCo fragment (15-26). For 3 we were treated with [CpCo(cod)]: 1-oxacyclotetradeca-4,11diyne (2), 1,8-dioxacyclotetradeca-4,11-diyne (3), cyclotetra-could isolate, besides the cyclobutadiene complex 16, the trimerization product 28.
📜 SIMILAR VOLUMES
The trichlorides of yttrium, samarium, and lutetium react with 2 equivalents of Na[C 5 H 4 t Bu] and 1 equivalent of NaBH 4 to give [(g 5 -C 5 H 4 t Bu) 2 LnBH 4 (THF)] (Ln = Y (1), Sm (2), Lu (3)) or with 2 equivalents of Na[C 5 Me 4 R] and 1 equivalent of NaBH 4 to form [(g 5 -C 5 Me 4 R) 2 ĹnBH 4
The reaction of cationic diolefinic rhodium(I) complexes with 2-(diphenylphosphino)benzaldehyde (pCHO) was studied. [Rh(cod) 2 ]ClO 4 (cod cycloocta-1,5-diene) reacted with pCHO to undergo the oxidative addition of one pCHO with (1,2,3-h)cyclooct-2-en-1-yl (h 3 -C 8 H 13 ) formation, and the coordin