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Tris(2,2'-bisimidazoline)cobalt(II) is a coordination complex compound with the chemical formula [Co(C9H12N4)3]. It consists of a central cobalt(II) ion (Co2+) coordinated to three 2,2'-bisimidazoline ligands. The 2,2'-bisimidazoline ligand is a bidentate ligand, meaning it can bind to the metal ion through two donor atoms, in this case, the nitrogen atoms of the imidazole rings. tris(2,2'-bisimidazoline)cobalt(II) is known for its potential applications in catalysis, particularly in the activation of small molecules like hydrogen and carbon monoxide. It is also of interest in the field of homogeneous catalysis due to its ability to stabilize metal centers in a specific geometry, which can influence the reactivity and selectivity of catalytic reactions. The compound's structure and electronic properties make it a subject of study in inorganic chemistry and materials science.

47664-14-2

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47664-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 47664-14-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,7,6,6 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 47664-14:
(7*4)+(6*7)+(5*6)+(4*6)+(3*4)+(2*1)+(1*4)=142
142 % 10 = 2
So 47664-14-2 is a valid CAS Registry Number.

47664-14-2Downstream Products

47664-14-2Relevant academic research and scientific papers

The importance of precursor and successor complex formation in a bimolecular proton-electron transfer reaction

Mader, Elizabeth A.,Mayer, James M.

, p. 3685 - 3687 (2010)

The transfer of a proton and an electron from the hydroxylamine 1-hydroxyl-2,2,6,6-tetramethylpiperidine (TEMPOH) to [CoIII(Hbim) (H2bim)2]2+ (H2bim = 2,2′-biimidazoline) has an overall driving force of ΔG° = -3.0 ± 0.4 kcal mol-1 and an activation barrier of ΔG ° = 21.9 ± 0.2 kcal mol-1. Kinetic studies implicate a hydrogen-bonded precursor complex at high [TEMPOH], prior to proton-electron (hydrogen-atom) transfer. In the reverse direction, [CoII(H2bim)3]2+ + TEMPO, a similar successor complex was not observed, but upper and lower limits on its formation have been estimated. The energetics of formation of these encounter complexes are the dominant contributors to the overall energetics in this system: ΔG°′ for the proton-electron transfer step is only -0.3 ± 0.9 kcal mol-1. Thus, formation of the precursor and successor complexes can be a significant component of the thermochemistry for intermolecular proton-electron transfer, particularly in the low-driving-force regime, and should be included in quantitative analyses.

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