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[Au(2,2'-bipyridyl)(PPh3)]PF6 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60898-06-8

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60898-06-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60898-06-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,9 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 60898-06:
(7*6)+(6*0)+(5*8)+(4*9)+(3*8)+(2*0)+(1*6)=148
148 % 10 = 8
So 60898-06-8 is a valid CAS Registry Number.

60898-06-8Downstream Products

60898-06-8Relevant academic research and scientific papers

Unsymmetrical Coordination of Bipyridine in Three-Coordinate Gold(I) Complexes

Adams, Alexandria V.,Aristov, Michael M.,Balch, Alan L.,Berry, John F.,Luong, Lucy M. C.,Olmstead, Marilyn M.,Walters, Daniel T.

, (2020)

The unsymmetrical coordination of gold(I) by 2,2′-bipyridine (bipy) in some planar, three-coordinate cations has been examined by crystallographic and computational studies. The salts [(Ph3P)Au(bipy)]XF6 (X = P, As, Sb) form an isomorphic series in which the differences in Au-N distances range from 0.241(2) to 0.146(2) ?. A second polymorph of [(Ph3P)Au(bipy)]AsF6 has also been found. Both polymorphs exhibit similar structures. The salts [(Et3P)Au(bipy)]XF6 (X = P, As, Sb) form a second isostructural series. In this series the unsymmetrical coordination of the bipy ligand is maintained, but the gold ions are disordered over two unequally populated positions that produce very similar overall structures for the cations. Although many planar, three-coordinate gold(I) complexes are strongly luminescent, the salts [(R3P)Au(bipy)]XF6 (R = Ph or Et; X = P, As, Sb) are not luminescent as solids or in solution. Computational studies revealed that a fully symmetrical structure for [(Et3P)Au(bipy)]+ is 7 kJ/mol higher in energy than the observed unsymmetrical structure and is best described as a transition state between the two limiting unsymmetrical geometries. The Au-N bonding has been examined by natural resonance theory (NRT) calculations using the 12 electron rule . The dominant Lewis structure is one with five lone pairs on Au and one bond to the P atom, which results in a saturated (12 electron) gold center and thereby inhibits the formation of any classical, 2 e- bonds between the gold and either of the bipy nitrogen atoms. The nitrogen atoms may instead donate a lone pair into an empty Au-P antibonding orbital, resulting in a three-center, four-electron (3c/4e) P-Au-N bond. The binuclear complex, [μ2-bipy(AuPPh3)2](PF6)2, has also been prepared and shown to have an aurophillic interaction between the two gold ions, which are separated by 3.0747(3) ?. Despite the aurophillic interaction, this binuclear complex is not luminescent.

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