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Tris-(tri-p-tolylphosphine)gold(I) perchlorate is a gold-based organometallic compound with the chemical formula [Au(P(C6H4-4-CH3)3)3]ClO4. It consists of a gold(I) center coordinated to three tri-p-tolylphosphine ligands, where each phosphine ligand is a trivalent phosphorus atom bonded to three p-tolyl (4-methylphenyl) groups. The perchlorate anion (ClO4-) is present to balance the overall charge of the complex. tris-(tri-p-tolylphosphine)gold(I) perchlorate is of interest in the field of homogeneous catalysis, particularly in the study of gold complexes due to their unique electronic properties and potential applications in various chemical transformations. The bulky tri-p-tolylphosphine ligands provide steric protection to the gold center, which can influence the reactivity and selectivity of the complex in catalytic processes.

79648-41-2

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79648-41-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79648-41-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,4 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79648-41:
(7*7)+(6*9)+(5*6)+(4*4)+(3*8)+(2*4)+(1*1)=182
182 % 10 = 2
So 79648-41-2 is a valid CAS Registry Number.

79648-41-2Downstream Products

79648-41-2Relevant academic research and scientific papers

Characterisation of Two-, Three-, and Four-co-ordinate Gold(I) Complexes by 197Au Moessbauer and 31P- Nuclear Magnetic Resonance Spectroscopy

Parish, R. V. ('Dick'),Parry, Owen,McAuliffe, Charles A.

, p. 2098 - 2104 (1981)

The isolation of some new three- and four-co-ordinate gold(I) complexes is reported. 197Au Moessbauer data are given for two-, three-, and four co-ordinate complexes, and the technique is shown to be well suited to the determination of co-ordination numbers.For the two- and three-co-ordinate systems the point-charge (partial quadrupole splitting) approach works well, provided that the structures are regular. 31P- n.m.r. data for the Au(1+)-P(C6H11)Ph2 system show that a maximum of three ligands can be bound to the cation.Data for this and other ligands are correlated with the ligand cone angles.Inconsistences between the species present in solution and those obtained by crystallisation are discussed.

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