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((NC5(CON(C2H5)2)H3)2)Pt(CCC6H4CH3)2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

357913-70-3

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357913-70-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 357913-70-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,7,9,1 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 357913-70:
(8*3)+(7*5)+(6*7)+(5*9)+(4*1)+(3*3)+(2*7)+(1*0)=173
173 % 10 = 3
So 357913-70-3 is a valid CAS Registry Number.

357913-70-3Upstream product

357913-70-3Downstream Products

357913-70-3Relevant academic research and scientific papers

Photophysics of diimine platinum(II) bis-acetylide complexes

Whittle,Weinstein,George,Schanze

, p. 4053 - 4062 (2001)

A comprehensive photophysical investigation has been carried out on a series of eight complexes of the type (diimine)Pt(-C≡C-Ar)2, where diimine is a series of 2,2′-bipyridine (bpy) ligands and -C≡C-Ar is a series of substituted aryl acetylide ligands. In one series of complexes, the energy of the Pt → bpy metal-to-ligand charge transfer (MLCT) excited state is varied by changing the substituents on the 4,4′- and/or the 5,5′-positions of the bpy ligand. In a second series of complexes the electronic demand of the aryl acetylide ligand is varied by changing the para substituent (X) on the aryl ring (X = -CF3, -CH3, -OCH3, and -N(CH3)2). The effect of variation of the substituents on the excited states of the complexes has been assessed by examining their UV-visible absorption, variable-temperature photoluminescence, transient absorption, and time-resolved infrared spectroscopy. In addition, the nonradiative decay rates of the series of complexes are subjected to a quantitative energy gap law analysis. The results of this study reveal that in most cases the photophysics of the complexes is dominated by the energetically low lying Pt ← bpy 3MLCT state. Some of the complexes also feature a low-lying intraligand (IL) 3π,π* excited state that is derived from transitions between π- and π*-type orbitals localized largely on the aryl acetylide ligands. The involvement of the IL 3π,π* state in the photophysics of some of the complexes is signaled by unusual features in the transient absorption, time-resolved infrared, and photoluminescence spectra and in the excited-state decay kinetics. The time-resolved infrared difference spectroscopy indicates that Pt ← bpy MLCT excitation induces a +25 to + 35 cm-1 shift in the frequency of the C≡C stretching band. This is the first study to report the effect of MLCT excitation on the vibrational frequency of an acetylide ligand.

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