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The chemical compound "(Rh(NH3)5(4-HO-hcn))(ClO4)3" is a coordination complex consisting of a rhodium(III) center. Rhodium is a transition metal that is often used in catalytic processes. In this complex, the rhodium ion is coordinated by five ammonia (NH3) molecules and one 4-hydroxy-2-cyanopyridine (4-HO-hcn) ligand, which is a type of heterocyclic compound with a hydroxyl group and a cyano group. The overall charge of the complex is balanced by three perchlorate (ClO4) ions, which are commonly used as counterions in coordination chemistry due to their stability and non-reactivity. This complex is of interest in the field of inorganic chemistry, particularly in the study of metal complexes and their potential applications in catalysis, sensing, and other areas.

76793-81-2

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76793-81-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76793-81-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,7,9 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76793-81:
(7*7)+(6*6)+(5*7)+(4*9)+(3*3)+(2*8)+(1*1)=182
182 % 10 = 2
So 76793-81-2 is a valid CAS Registry Number.

76793-81-2Relevant academic research and scientific papers

Intramolecular energy transfer in a rhodium(III) metalloorganic bichromophore system. Photochemical and photoluminescence studies

Bergkamp, Michael A.,Watts, Richard J.,Ford, Peter C.

, p. 1764 - 1767 (2008/10/08)

Reported are the photochemical, photoluminescence, and spectral studies of a series of pentaammine(organonitrilo)rhodium(III) compounds, Rh(NH3)5(N≡C-R)3+ (where R is a phenyl, benzyl, or 2-phenylethyl group or a substituted derivative). The absorption spectroscopy exhibits features attributable to both ππ* and ligand field transitions. The luminescence spectra, however, exhibit only ligand field (LF) emissions regardless of whether the ππ* or LF states are initially populated. The luminescence lifetimes at 77 K are also characteristic of LF states. Irradiation of the ππ* or LF bands in aqueous solutions leads to photosubstitution of the organonitrile ligand with the quantum yields being somewhat smaller for λirr = 254 nm (ππ*) than 313 nm (LF) in most cases. The results are discussed in terms of the efficiency of interconfigurational energy transfer between ππ* and LF states.

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