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4,7-diphenyl-1,10-phenanhroline 3,5-di-tert-butylbenzene-1,2-dithiolate platinum(II) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

220177-62-8

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220177-62-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220177-62-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,1,7 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 220177-62:
(8*2)+(7*2)+(6*0)+(5*1)+(4*7)+(3*7)+(2*6)+(1*2)=98
98 % 10 = 8
So 220177-62-8 is a valid CAS Registry Number.

220177-62-8Downstream Products

220177-62-8Relevant academic research and scientific papers

On the second-order nonlinear optical structure-property relationships of metal chromophores

Base, Karel,Tierney, Mark T.,Fort, Alain,Muller, Jacques,Grinstaff, Mark W.

, p. 287 - 289 (1999)

The synthesis and solvent-dependent second-order polarizability, β, responses of three new platinum(II) chromophores are reported. A strong correlation between the metal chromophore electronic structure and the second-order polarizability is observed that substantiates the use of the two-state model to design, optimize, and study new NLO chromophores.

Probing the electronic structure of platinum(II) chromophores: Crystal structures, NMR structures, and photophysical properties of six new bis- and di- phenolate/thiolate Pt(II)diimine chromophores

Weinstein, Julia A.,Tierney, Mark T.,Davies, E. Stephen,Base, Karel,Robeiro, Anthony A.,Grinstaff, Mark W.

, p. 4544 - 4555 (2009/06/17)

A general route for synthesis of six structurally similar Pt(II) diimine thiolate/phenolates chromophores possessing bulky phenolate or thiolate ligands is reported. The Pt chromophores were characterized using an array of techniques including 1H, 13C, and 195Pt NMR, absorption, emission, (spectro)electrochemistry, and EPR spectroscopy. Systematic variation of the electronic structure of the Pt(II) chromophores studied was achieved by (i) changing solvent polarity; (ii) substituting oxygen for sulfur in the donor ligand; (iii) alternating donor ligands from bis- to di-coordination; and (iv) changing the electron donating/withdrawing properties of the ligand(s). The lowest excited state in these new chromophores was assigned to a [charge-transfer-to-diimine] transition from the HOMO of mixed Pt/S (or Pt/O) character on the basis of absorption and emission spectroscopy, UV/vis (spectro)electrochemistry, and EPR spectroscopy. One of the chromophores, Pt(dpphen)(3,5-di-tert-butyl-catecholate) represents an example of a Pt-(II) diimine phenolate chromophore that possesses a reversible oxidation centered predominantly on the donor ligand. Results from EPR spectroscopy indicate participation of the Pt(II) orbitals in the HOMO. There is a dramatic difference in the photophysical properties of carborane complexes compared to other mixed-ligand Pt(II) compounds, which includes room-temperature emission and photostability. The charge-transfer character of the lowest excited state in this series of chromophores is maintained throughout. Moreover, the absorption and emission energies and the redox properties of the excited state can be significantly tuned.

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