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[Cu(N-[2-(4-(dimethylamino)-pyridin-2-yl)-ethyl]-N,N',N'-trimethyl-propane-1,3-diamine)][B(C6F5)4] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

883885-05-0

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883885-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 883885-05-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,3,8,8 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 883885-05:
(8*8)+(7*8)+(6*3)+(5*8)+(4*8)+(3*5)+(2*0)+(1*5)=230
230 % 10 = 0
So 883885-05-0 is a valid CAS Registry Number.

883885-05-0Relevant articles and documents

Copper-dioxygen adducts and the side-on peroxo dicopper(II)/bis(μ-oxo) dicopper(III) equilibrium: Significant ligand electronic effects

Hatcher, Lanying Q.,Vance, Michael A.,Sarjeant, Amy A. Narducci,Solomon, Edward I.,Karlin, Kenneth D.

, p. 3004 - 3013 (2008/10/09)

The variation of ligand para substituents on pyridyl donor groups of tridentale amine copper(I) complexes was carried out in order to probe electronic effects on the equilibrium between μ-η2:η2-(side-on)-peroxo [Cu2II(O22-)]2+ and bis(μ-oxo) [Cu2III(O2-)2] species formed upon reaction with O2. [CuI(R-PYAN)(MeCN)n]B(C6F5) 4 (R-PYAN = N-[2-(4-R-pyridin-2-yl)-ethyl]-N,N′,N′-trimethyl-propane-1,3- diamine, R = NMe2, OMe, H, and Cl) (1R) vary over a narrow range in their CuII/CuI redox potentials (E1/2 vs Fe(cp)2+/0 = -0.40 V for 1NMe2, -0.38 V for 1OMe, -0.33 V for 1H, and -0.32 V for 1Cl) and in C-O stretching frequencies of their carbonyl adducts, 1R-CO: ν(C-O) = 2080, 2086, 2088, and 2090 cm-1 for R = NMe2, OMe, H, and Cl, respectively. However, within this range of electronic properties for 1R, dioxygen reactivity is significantly affected. The reaction of 1Cl or 1H with O2 at -78°C in CH2Cl2 gives UV-vis and resonance Raman spectra indicative of a μ-η2:η2-(side-on)-peroxo dicopper(II) adduct (2R). Compound 1OMe reacts with O2, yielding equilibrium mixtures of side-on peroxo (2OMe) and bis(μ-oxo) (3OMe) species. Oxygenation of 1NMe2 leads to the sole generation of the bis(μ-oxo) dicopper(III) complex (3NMe2). A solvent effect was also observed; in acetone or THF, increased ratios of bis(μ-oxo) relative to side-on peroxo complex are observed. Thus, the equilibrium between a dicopper side-on peroxo and bis(μ-oxo) species can be tuned by ligand design-specifically, more electron donating ligands favor the formation of the latter isomer, and the peroxo/bis-(μ-oxo) equilibrium can be shifted from one extreme to the other within the same ligand system. Observations concerning the reactivity of the dioxygen adducts 2H and 3NMe2 toward external substrates are also presented.

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