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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 2165-2170 
    ISSN: 0009-2940
    Keywords: Titanocene complexes ; Zirconocene complexes ; Cyclopropene complexes ; Metallacyclobutenes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Metallacyclobutenes via η2-Cyclopropene Complexes of Titanocene and Zirconocene(η2-Cyclopropene)(trimethylposphane) complexes of titanocene (4, 5) and zirconocene (8) are obtained in good yields by the reaction of 1,2-diphenylcyclopropene (2) or 4,8-dioxaspiro[2.5]oct-1-ene (3) with bis(trimethylphosphane)titanocene (1) and (1-butene)(trimethylphosphane)zirconocene (7), respectively. In solution the new complexes 4 and 8 rearrange smoothly above room temperature to give the metallacyclobutene derivatives 6 and 9. All new compounds were characterized by spectroscopic methods (31P, 1H, 13C NMR), and the crystal structure of 9 was determined by an X-ray analysis.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1541-1550 
    ISSN: 0009-2940
    Keywords: Titanocene complexes ; Zirconocene complexes ; Metallabicyclo[3.1.0]hexenes ; 4-Vinyl-1-metallacyclobutenes ; Oxidative coupling of alkynes with cyclopropenes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Metallabicyclo[3.1.0]hexenes and Their Rearrangement to Vinylmetallacyclobutenes (M=Ti, Zr)Alkyne-metallocene complexes, e.g. the alkynetitanocenes 1a, b, the alkyne(trimethylphosphane)titanocenes 2a, b and the alkyne(trimethylphosphane)zirconocenes 5a-d react readily with 3,3-dimethylcyclopropene (3a) and 3,3-diphenylcyclopropene (3b) to give the corresponding bis(η5-cyclopentadienyl)-metallabicyclo[3.1.0]hexene derivatives 4a-e, (M=Ti) and 6a-g (M=Zr) in high yields. In an analogous manner, metallabicyclo[3.1.0]hexene derivatives of Ti or Zr can be prepared from 1,2-diphenylcyclopropene(trimethylphosphane)metallocenes 9 and 10 and 2-butyne to yield 11 and 12 and from benzyne 3a or 3b to yield 8a and 8b. Some of these metallabicyclo[3.1.0]hexene derivatives rearrange quantitatively to the corresponding 4-(dimethylvinyl)-1-metalla-2-cyclobutene derivates 16 and 17a and 4-(diphenylvinyl)-1-metalla-2-cyclobutenes 15c and 17a-c when they are heated to 60-80°C for several hours. The 4-(diphenylvinyl)-1-titana-2-cyclobutene derivatives 15a-c can also be obtained by reaction of [(2,2-diphenylvinyl)carbene](trimethylphosphane)-titanocen (13) with disubstituted alkynes such as tolane, phenyltrimethylsilylacetylene and bis(trimethylsily)acetylene. With other alkynes, e.g. 2-butyne, 1-butyne, 1-propyne or acetylene, 13 reacts by polymerization of these alkynes; the corresponding 4-vinyl-1-titanacyclobutene derivatives could not be detected in the reaction mixture. All new metallacycles are fully characterized by spectroscopic methods, extensive 1H- and 13C-NMR studies provide unambiguous proof of their structures.
    Additional Material: 6 Tab.
    Type of Medium: Electronic Resource
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