1988
DOI: 10.1016/0022-328x(88)80096-2
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Koordination und Chemie von Acetylenen an dicarbonylbis(tirmethlphosphit)eisen-fragmenten

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Cited by 33 publications
(13 citation statements)
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“…[53][54][55][56] These molecules are structurally quite similar to 43-45. It is interesting to note that the authors did not report these complexes as aromatic, though they do have some characteristics suggesting that delocalization is present.…”
Section: Osmabenzofuranmentioning
confidence: 94%
“…[53][54][55][56] These molecules are structurally quite similar to 43-45. It is interesting to note that the authors did not report these complexes as aromatic, though they do have some characteristics suggesting that delocalization is present.…”
Section: Osmabenzofuranmentioning
confidence: 94%
“…Although examples of these compounds are still relatively rare as well, the large possible number of variationsi nr ing size, heteroatom choice, degree of saturation and substitution (as well as possible isomers) suggests this could potentially developi nto av ery large set of compounds. Compounds in this class that have already been reported [117] include metallabenzothiirenes, [37,46,78] metallabenzoxirenes, [59,129] metallabenzazirines [59] metallabenzofurans, [91,[130][131][132][133][134] metallabenzothiophenes, [73,135] metallabenzothiazole, [52] metallabenzothiazolium, [78] and metallabenzoxathioles. [59,117] Formation of the ruthenabenzothiophene dimer 24,( am etalla-analogue of benzo[b]thiophene) was recently reportedt o occur via CÀHa ctivation of the thiophenes ubstituent of ac oordinated vinyl carbene ligand.…”
Section: Fused-ring Metallabenzenesmentioning
confidence: 99%
“…Although examples of these compounds are still relatively rare as well, the large possible number of variations in ring size, heteroatom choice, degree of saturation and substitution (as well as possible isomers) suggests this could potentially develop into a very large set of compounds. Compounds in this class that have already been reported include metallabenzothiirenes, metallabenzoxirenes, metallabenzazirines metallabenzofurans, metallabenzothiophenes, metallabenzothiazole, metallabenzothiazolium, and metallabenzoxathioles …”
Section: Metallabenzenesmentioning
confidence: 99%
“…A related complex 165, which can be described as a fused-ring metallacyclohexadiene, was identified as the major product when 162 was chosen as the reactant (Scheme 52). 205,206 As mentioned in section 3.1.2, one of the methods to synthesize η 6 -coordinated metallabenzenes is a direct method which does not use free metallabenzenes, and the synthesis of several η 6 -ruthenabenzenes has been described. This methodology can also be extended for the synthesis of metallabenzenes based on other metals.…”
Section: Synthesis Of Metallabenzenes Based On Othermentioning
confidence: 99%