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tricarbonyl(κ1-triflate)manganese(I)(PPh(OEt)2)2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

186344-34-3

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186344-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 186344-34-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,3,4 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 186344-34:
(8*1)+(7*8)+(6*6)+(5*3)+(4*4)+(3*4)+(2*3)+(1*4)=153
153 % 10 = 3
So 186344-34-3 is a valid CAS Registry Number.

186344-34-3Downstream Products

186344-34-3Relevant academic research and scientific papers

Preparation of diethylcyanamide and cyanoguanidine complexes of manganese and rhenium

Albertin, Gabriele,Antoniutti, Stefano,Castro, Jesús,Siddi, Silvio

, p. 83 - 90 (2014)

Diethycyanamide complexes [M(NCNEt2)(CO)nL 5-n]BPh4 (1a-5a) [M = Mn, Re; n = 1, 2, 3; L = PPh(OEt)2, P(OEt)3] were prepared by allowing hydrides MH(CO)nL5-n to react f

Synthesis, characterization, and reactivity of cationic molecular hydrogen complexes of manganese(I)

Albertin, Gabriele,Antoniutti, Stefano,Bettiol, Massimo,Bordignon, Emilio,Busatto, Fabio

, p. 4959 - 4969 (2008/10/08)

Hydride complexes MnH(CO)3P2 (1), MnH(CO)2P3 (2), and MnH(CO)P4 (3) (P = P(OEt)3 (a), PPh(OEt)2 (b), PPh2OEt (c), PPh(OiPr)2 (d) were prepared by allowing the MnH(CO)5 species to react with an excess of phosphine upon UV irradiation or under reflux conditions. Their formulation and geometry in solution were established by IR and 1H, 13C, and 31P NMR spectroscopy. Protonation reactions with HBF4·Et2O of the monocarbonyls MnH(CO)-P4 (3) afford isolable dihydrogen derivatives [Mn(η2-H2)(CO)P4]BPh4 (5), which were characterized by variable-temperature 1H and 31P NMR spectra, T1 measurements, and JHD values. Thermally unstable (above 0°C) [Mn(η2-H2)(CO)2P3]+ (4) cations were also prepared by protonation of the dicarbonyl hydrides MnH(CO)2P3 (2) and fully characterized in solution. Evolution of H2 from 4 and 5 results in the formation of the unsaturated complexes [Mn-(CO)2P3]BPh4 (6) and [Mn(CO)P4]BPh4 (7), which are probably stabilized by an agostic interaction between the metal center and a C-H proton of the phosphite. Treatment of the unsaturated complexes 6 and 7 and of the triflate compounds [Mn(η1-OSO2CF3)(CO)3P 2] (8) with Li+RC≡C- gave the new acetylide derivatives [Mn(C≡CR)(CO)P4] (9), [Mn(C≡CR)-(CO)2P3] (10), and [Mn(C≡CR)(CO)3P2] (11) (R = Ph, p-tolyl). The new series of cationic manganese compounds [Mn(CO)2(p-tolylCN)P3]BPh4 (12), [Mn(CO)(p-tolylCN)P4]BPh4 (13), [Mn(CO)2(p-tolylNC)P3]BPh4 (14), [Mn(CO)(p-tolylNC)P4]BPh4 (15), [Mn(CO)3P3]BPh4 (16), and [Mn(CO)2P4]BPh4 (17) were also obtained by reacting the unsaturated compounds 6 and 7 with the appropriate ligands.

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