Benzylidene-bis(tricyclohexylphosphine)dichlororuthenium

Bezeichnung:Benzylidene-bis(tricyclohexylphosphine)dichlororuthenium

CAS-Nr172222-30-9

Englisch Name:Benzylidene-bis(tricyclohexylphosphine)dichlororuthenium

CBNumberCB0296067

SummenformelC43H73Cl2P2Ru

Molgewicht823.96

MOL-Datei172222-30-9.mol

Benzylidene-bis(tricyclohexylphosphine)dichlororuthenium physikalisch-chemischer Eigenschaften

Schmelzpunkt	153 °C (dec.)(lit.)
storage temp.	2-8°C
Löslichkeit	Chloroform (Slightly), Dichloromethane (Sparingly)
Aggregatzustand	solid
Farbe	Purple
Merck	13,4565
InChI	InChI=1S/2C18H33P.C7H5.2ClH.Ru/c21-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;1-7-5-3-2-4-6-7;;;/h216-18H,1-15H2;2-6H;2*1H;/q;;-2;;;+2
InChIKey	PNPBGYBHLCEVMK-UHFFFAOYSA-L
SMILES	[Ru+4]([Cl-])([Cl-])(=[C-2]C1C=CC=CC=1)(P(C1CCCCC1)(C1CCCCC1)C1CCCCC1)P(C1CCCCC1)(C1CCCCC1)C1CCCCC1
CAS Datenbank	172222-30-9

Sicherheit

Kennzeichnung gefährlicher	Xi,F
R-Sätze:	36/37/38-11
S-Sätze:	26-36
RIDADR	1325
WGK Germany	3
F	10-23
HazardClass	4.1
PackingGroup	Ⅱ
HS Code	28439000

Gefahreninformationscode (GHS)

Benzylidene-bis(tricyclohexylphosphine)dichlororuthenium Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
S-Sätze Betriebsanweisung:
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
Beschreibung
Phenylmethylenebis(tricyclohexylphosphorus)ruthenium dichloride is a ruthenium catalyst. Ruthenium catalysts are highly resistant to polar monomers, enabling the polymerization of many polar monomers to prepare cyclic olefin copolymers. Cyclic olefin copolymers can be widely used in the manufacture of various optical, information, electrical, and medical materials.
Chemische Eigenschaften
bright purple powder
Verwenden
First metathesis catalyst to be widely used in organic synthesis. Useful for acyclic diene metathesis polymerization (ADMET), Ring-Opening Metathesis Polymerization (ROMP) of strained cyclic olefins, ring opening metathesis (ROM), olefin cross metathesis (CM) and ring closing metathesis (RCM) of terminal olefins under a variety of reactions conditions.
Verwenden
Catalysis of olefin metathesis including ring-closing of dienes, cross metathesis and ring-opening methathesis polymerizations (ROMP).
Verwenden
suzuki reaction
Application
Phenylmethylenebis(tricyclohexylphosphorus)ruthenium dichloride can be widely used in organic synthesis, the first metathesis catalyst; under a wide range of reaction conditions, it is effective for the ring-opening metathesis of strained cyclic olefins of terminal olefins Polymerization, cross-metathesis and ring-closure metathesis units of olefins and vinyl alcohol decomposition of internal olefins.
reaction suitability
reagent type: catalyst
core: ruthenium
reaction type: Ring-Opening Polymerization
läuterung methode
Wash it repeatedly with Me2CO and MeOH and dry it in a vacuum. Alternatively dissolve it in CH2Cl2, concentrate it to half its volume, filter, add MeOH to precipitate it as purple microcrystals. Filter these off, wash several times with Me2CO and MeOH and dry them in a vacuum for several hours. [Scwab et al. J Am Chem Soc 118 100 1996, Miller et al. J Am Chem Soc 118 9606 1996, Furstner & Langermann J Am Chem Soc 119 9130 1997.] § A polymer supported version is available [Schwab et al. Angew Chem (Intl Edn) 34 2039 1995.].

Benzylidene-bis(tricyclohexylphosphine)dichlororuthenium Upstream-Materialien And Downstream Produkte

Benzylidene-bis(tricyclohexylphosphine)dichlororuthenium Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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