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92669-43-7

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  • Carbonyl[5,10,15,20-tetrakis(2,4,6-trimethylphenyl)-21H,23H-porphinato] ruthenium(II), min. 98%

    Cas No: 92669-43-7

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92669-43-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92669-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,6,6 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 92669-43:
(7*9)+(6*2)+(5*6)+(4*6)+(3*9)+(2*4)+(1*3)=167
167 % 10 = 7
So 92669-43-7 is a valid CAS Registry Number.

92669-43-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (5,10,15,20-tetramesitylporphyrinate)ruthenium(II) carbonyl complex

1.2 Other means of identification

Product number -
Other names CARBONYL[5,10,15,20-TETRAKIS(2,4,6-TRIMETHYLPHENYL)-21H,23H-PORPHINATO]RUTHENIUM(II)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:92669-43-7 SDS

92669-43-7Relevant articles and documents

Sandwich structure of a ruthenium porphyrin and an amino acid hydrazide for probing molecular chirality by circular dichroism

Liang, Qing-Feng,Liu, Juan-Juan,Chen, Jian

supporting information; experimental part, p. 3987 - 3991 (2011/08/09)

Owing to the strong Lewis acidity of ruthenium porphyrins, a commercial carbonyl ruthenium porphyrin and an amino acid hydrazide can assemble into a sandwich structure. The nature of such a structure is diagnostic of the absolute configuration of the amino acid by circular dichroism.

Synthesis and properties of metalloporphyrin monolayers and stacked multilayers bound to an electrode via site specific axial ligation to a self- assembled monolayers

Offord, David A.,Sachs, Sandra B.,Ennis, Matthew S.,Eberspacher, Todd A.,Griffin, John H.,Chidsey, Christopher E. D.,Collman, James P.

, p. 4478 - 4487 (2007/10/03)

A general method has been developed for the immobilization of metalloporphyrins at a gold electrode surface coated with a self-assembled monolayers (SAM). SAMs containing imidazole-terminated adsorbates are shown to bind a series of metalloporphyrins, including bis-acetonitrile octaethylporphyrinatoruthenium (II), Ru(OEP)(CH3CN)2; bis-acetonitrile octaethyltetraazaporphyrinato ruthenium(II), Ru(OETAP)(CH3CN)2, bis- acetonitrile tetra-(p-chlorophenyl)porphyrinatoruthrnium(II), Ru(Tp- CIPP)(CH3CN)2, bis-acetonitrile octaethylporphtrinatoosmium(II), Os(OEP)(CH3CN)2, and carbonyl meso-tetramesitylporphyrinatoruthenium(II), Ru(TMP)(CO). The SAM/metalloporphyrin films have been characterized by optical ellipsometry, contact angle goniometry, X-ray photoelectron spectroscopy, grazing angle FT-IR spectroscopy, transmission visible spectroscopy, and electrochemistry. The results indicated that the metalloporphyrins are chemisorbed via axial ligand substitution of the metal center with the porphyrin ring parallel to the surface and the second axial ligand position normal to the surface. Scanning tunneling microscopy images of Ru(TMP)(CO) bound to the SAM corroborate this model. Axial ligation of metalloporpyrins to SAMs serves as the basis for an iterative, defined approach to the preparation of stacked single component and mixed metalloporphyrin multilayers on SAms. In these materials, the bidentate ligand pyrazine serves as a bridge between successive metalloporphyrins in the stacks.

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