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[platinum(II)(terpyridine)(phenylacetylide)] chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1184830-87-2

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1184830-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1184830-87-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,4,8,3 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1184830-87:
(9*1)+(8*1)+(7*8)+(6*4)+(5*8)+(4*3)+(3*0)+(2*8)+(1*7)=172
172 % 10 = 2
So 1184830-87-2 is a valid CAS Registry Number.

1184830-87-2Relevant academic research and scientific papers

Luminescent Pt(2,6-bis(: N -methylbenzimidazol-2-yl)pyridine)X+: A comparison with the spectroscopic and electrochemical properties of Pt(tpy)X+(X = Cl, CCPh, Ph, or CH3)

Connick, William B.,Grove, Levi J.,Shingade, Vikas M.

, p. 9651 - 9661 (2020)

A series of platinum(ii) pincer complexes of the formula Pt(mbzimpy)X+, 1(a-d), (mbzimpy = 2,6-bis(N-methylbenzimidazol-2-yl)pyridine; X = Cl; (a), CCPh; (b), Ph; (c), or CH3; (d), CCPh = phenylacetylide, and Ph = Phenyl) have been synthesized and characterized. Electronic absorption and emission, as well as electrochemical properties of these compounds, have been investigated. Pt(tpy)X+ analogs (tpy = 2,2′;6′2′′-terpyridine), 2(a-d), have also been investigated and compared. Electrochemistry shows that 1 and 2 analogs undergo two chemically reversible one-electron reduction processes that are shifted cathodically along the a b c d series. Notably, these reductions occur at slightly higher negative potentials in the case of 1. The absorption spectra of 1 and 2 in acetonitrile exhibit ligand-centered (1LC) transitions (? ≈ 104 M-1 cm-1) in the UV region and metal-to-ligand-charge transfer (1MLCT) transitions (? ≈ 103 M-1 cm-1) in the visible region. The corresponding visible bands of 1b and 2b have been assigned to 1(LLCT/MLCT) mixed state (LLCT: ligand-to-ligand-charge transfer). The preceding 1LC and 1MLCT transitions of 1 occur at lower energies than that of 2. These 1LC transitions have distinctly been blue-shifted along a c d in 2, but occur at nearly identical energies in 1. Conversely, 1MLCT transitions are red-shifted along a c d in both the analogs. The 77 K glassy solutions of 1 and 2 exhibit an intense vibronically-structured emission band at λmax(0-0) in the 470-560 nm range. This band is red-shifted along b a ≤ c d in 1 and along a ≤ d ≈ c ? b in 2. The main character of these emissions is assigned to 3LLCT emissive state in 1b and 2b, whereas to 3LC in the rest of the compounds. Relative stabilization of these spin-forbidden emissive states is discussed by invoking configuration mixing with the higher-lying 3MLCT state.

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