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Bis(tricyclohexylphosphine)[(phenylthio)methylene]ruthenium(II) dichloride, min. 97%

Catalog Number
ACM219770997-1
Product Name
Bis(tricyclohexylphosphine)[(phenylthio)methylene]ruthenium(II) dichloride, min. 97%
Structure
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CAS
219770-99-7
  • Product Overview
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Synonyms
Bis(tricyclohexylphosphine)[(phenylthio)methylene]ruthenium(IV) dichloride; SCHEMBL995991; BIS(TRICYCLOHEXYLPHOSPHINE)[(PHENYLTHIO)METHYLENE]RUTHENIUM(II) DICHLORIDE; Bis(tricyclohexylphosphine)[(phenylthio)methylene]ruthenium(II)dichloride; SC10225; 437767-65-2;
IUPAC Name
dichloro(phenylsulfanylmethylidene)ruthenium;tricyclohexylphosphane;
Molecular Weight
855.027g/mol
Molecular Formula
C43H72Cl2P2RuS;
Canonical SMILES
C1CCC(CC1)P(C2CCCCC2)C3CCCCC3.C1CCC(CC1)P(C2CCCCC2)C3CCCCC3.C1=CC=C(C=C1)SC=[Ru](Cl)Cl;
InChI
InChI=1S/2C18H33P.C7H6S.2ClH.Ru/c2*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;1-8-7-5-3-2-4-6-7;;;/h2*16-18H,1-15H2;1-6H;2*1H;/q;;;;;+2/p-2;
InChI Key
UDWHYAPPVOEOMP-UHFFFAOYSA-L;
Complexity
341
Covalently-Bonded Unit Count
3
Exact Mass
854.325g/mol
H-Bond Acceptor
1
Heavy Atom Count
49
Monoisotopic Mass
854.325g/mol
Rotatable Bond Count
8
Topological Polar Surface Area
25.3A^2
Application
Bis(tricyclohexylphosphine)[(phenylthio)methylene]ruthenium(II) dichloride, with a minimum purity of 97%, serves as a highly effective metathesis catalyst known for its stability in air and compatibility with aqueous media. It is particularly favored for the ring-opening metathesis polymerization of cycloolefins, where it operates efficiently at concentrations 2-3 times lower than comparable phenyl and vinyl-substituted ruthenium carbenes. Additionally, this catalyst acts as an excellent initiator for solvent-free polymerization, providing precise control over initiation rates and gelation times. Its high selectivity also makes it ideal for the ring opening and cross-metathesis of norbornene derivatives.
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