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940348

Dichloro(p-cymene)ruthenium(II) dimer ChemBeads

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동의어(들):

(p-Cymene)ruthenium(II) chloride dimer ChemBeads, Benzene-1-methyl-4-(1-methylethyl)-ruthenium complex ChemBeads

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About This Item

실험식(Hill 표기법):
C20H28Cl4Ru2
CAS Number:
Molecular Weight:
612.39
UNSPSC 코드:
12352100

형태

solid

Quality Level

구성

, 4-6 wt. % (loading)

반응 적합성

reagent type: catalyst

SMILES string

[Cl-][Ru+2]123456([Cl-][Ru+2]789%10%11([Cl-])([Cl-]1)[CH]=%12[CH]%11=C%10(C(C)C)[CH]9=[CH]8C%127C)[CH]=%13[CH]6=C5(C(C)C)[CH]4=[CH]3C%132C

InChI

InChI=1S/2C10H14.4ClH.2Ru/c2*1-8(2)10-6-4-9(3)5-7-10;;;;;;/h2*4-8H,1-3H3;4*1H;;/q;;;;;;2*+2/p-4

InChI key

LAXRNWSASWOFOT-UHFFFAOYSA-J

일반 설명

The ChemBeads product of the (p-Cymene)ruthenium(II) chloride dimer. Loaded at 5% wt. on glass beads for use in high-throughput expermentation (HTE).
Dichloro(p-cymene)ruthenium(II) dimer is commonly used as a ruthenium starting material, and has been used in:
- Bifunctional P-containing RuO2 catalysts prepared from surplus Ru coordination complexes applied to Zn/Air batteries.
- The synthesis of half-sandwich type platinum-group metal complexes of C-glucosaminyl azines.
- The C(sp2)-H bond functionalization along with concomitant (4+2) annulation of coumarin-3-carboxamide.
-The acceptor engineering of ruthenium metallocycles with high phototoxic indices for safer photodynamic therapy.

특징 및 장점

ChemBeads are chemical coated glass beads. ChemBeads offer improved flowability and chemical uniformity perfect for automated solid dispensing and high-throughput experimentation. The method of creating ChemBeads uses no other chemicals or surfactants allowing the user to accurately dispense sub-milligram amounts of chemical.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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An innovative synthetic route that involves the thermal treatment of selected Ru co-ordination complexes was used to prepare RuO2-based materials with catalytic activity for oxygen reduction (ORR) and oxygen evolution (OER) reactions. Extensive characterization confirmed the presence of Ru metal
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Organic & biomolecular chemistry, 21(27), 5567-5586 (2023-06-26)
Efficacious protocols have been established to synthesize a structurally privileged Π-extended coumarin-fused pyridone nucleus by activating the vinylic C(sp2)-H bond of coumarin-3-carboxamide under the influence of inexpensive Ru(II)-metal. Here an N-methoxy carboxamide entity has been exploited as the chelating fragment
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