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The chemical compound "[Rh(CO)(P(C6H11)3)2(mqa)][ClO4] mqa" is a rhodium-based complex with a unique structure. It features a rhodium (Rh) atom at its center, coordinated with a carbon monoxide (CO) ligand and two phosphine ligands, each of which is attached to a phenyl group (C6H11). The abbreviation "mqa" likely stands for a specific organic ligand or anion, which is not fully specified in the given formula. The compound also includes a perchlorate ion ([ClO4]-) as a counterion, which balances the overall charge of the complex. This complex is of interest in the field of organometallic chemistry, potentially for its catalytic properties or electronic structure, and the "mqa" ligand could influence its reactivity and stability.

75215-31-5

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75215-31-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75215-31-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,1 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75215-31:
(7*7)+(6*5)+(5*2)+(4*1)+(3*5)+(2*3)+(1*1)=115
115 % 10 = 5
So 75215-31-5 is a valid CAS Registry Number.

75215-31-5Downstream Products

75215-31-5Relevant academic research and scientific papers

Rhodium(I) Complexes of 8-Methyl-, 8-Ethyl-, and 8-Isopropyl-quinolines and Realated 2-Substituted Derivatives

Deeming, Antony J.,Rothwell, Ian P.

, p. 1259 - 1264 (2007/10/02)

The complexes have been prepared from on adding unidentate L (8-methyl-, -ethyl-, or -isopropyl-quinoline) or bidentate L (1,10-phenantroline or quinoline-2-carboxaldehide-N-methylimine). 8-Alkyl-substitution of the latter ligand gives the complexes as isomers with uni- and bi-dentate L respectively with relative stabilities of the unidentate form depending on the 8-substituent in the order Pri > Et > Me.Unidentate L is also favoured by replacing PPh3 by P(C6H11)3 but bidentate co-ordination is found using AsPh3 or PMe2Ph.Equilibrium constants for chloro-bridge cleavage of by 8-substituted and 2,8-disubstituted quinolines are reduced by increasing the size of the 8-susbtituent and even more by further introduction of a 2-methyl group.The contributions of distortions in the co-ordination to these changes in equilibrium constants are discussed.

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