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{triethylammonium}{closo-3-(triphenylphosphine)-3,3-(Cl)2-3,1,2-RhC2B9H11} is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87226-27-5

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87226-27-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87226-27-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,2 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 87226-27:
(7*8)+(6*7)+(5*2)+(4*2)+(3*6)+(2*2)+(1*7)=145
145 % 10 = 5
So 87226-27-5 is a valid CAS Registry Number.

87226-27-5Downstream Products

87226-27-5Relevant academic research and scientific papers

Synthesis of metallacycles by 1,3-dipolar cycloaddition reactions between low-valent metal carbonyls and aryl nitrile N-oxides

Chetcuti, Peter A.,Walker, John A.,Knobler, Carolyn B.,Hawthorne, M. Frederick

, p. 641 - 650 (2008/10/08)

Reaction of low-valent metal carbonyl complexes with aryl nitrile N-oxides leads to the synthesis of novel five-membered metallacycles by 1,3-dipolar cycloaddition of the aryl nitrile N-oxide to the M-CO bond of the low-valent metal carbonyl complex. The syntheses of these metallacycles from metallacarborane carbonyl anions [closo-3-PPh3-3-(CO)-3,1,2-MC2B9H 11]- (M = Ir, Rh) and [closo-2-PPh3-2-(CO)-2,1,7-RhC2B9H 11]- and a number of pentamethylcyclopentadienyl and cyclopentadienyl complexes of Co, Rh, and Ir of the type (η5-C5R5)LM(CO) (R = H, Me; L = PPh3, PMe3, CO) and the metal carbonyl anions M(CO)5- (M = Mn, Re) are described. The syntheses of these metallacycles proceed in good yield (50-85%). The factors influencing the chemical and thermal stability of these metallacycles are discussed, and single-crystal X-ray diffraction studies of the metallacycles [PPN] [closo-2-(PPh3)-2-{η2-C(m-FC6H 4)-NOC(=O)-}-2,1,7-RhC2B9H11] ([PPN]·5b) and (η5-C5Me5)(PMe3)Rh{η 2-C(p-FC6H4)NOC(=O)-} (9) are reported and their structures discussed. Crystallographic data for 9: space group P21/c; a = 9.0376 (7) A?, b = 14.8675 (13) A?, c = 16.1965 (14) A?, β = 99.074 (3)°, V = 2149 A?3, and Z = 4. For PPN·5b: space group P1; a = 12.910 (5) A?, b = 13.270 (5) A?, c = 18.402 (7) A?, α = 88.24 (3)°, β = 109.46 (3)°, γ = 83.89 (3)°, V = 2948 A?3, and Z = 2.

Synthesis and characterization of anionic halogen-containing rhodacarboranes. Crystal and molecular structure of the hydrogen-bonded ion pair [HPPh3][closo-3-Ph3P-3,3-Br2-3,1,2-RhC 2B9H11]

Zheng, Limin,Baker, R. Thomas,Knobler, Carolyn B.,Walker, John A.,Hawthorne, M. Frederick

, p. 3350 - 3355 (2008/10/08)

The title compound was obtained in low yield from the reaction of closo-3,3-(Ph3P)2-3-H-3,1,2-RhC2B 9H11 (1) and BBr3 and was characterized by an X-ray diffraction study. Red crystals of [HPPh3][closo-3-Ph3P-3,3-Br2-3,1,2-RhC 2B9H11]·1.5C6H6, [HPPh3][3]·1.5C6H6, were triclinic, space group P1, with a = 12.591 (5) A?, b = 13.299 (4) A?, c = 17.568 (5) A?, α = 111.77 (2)°, β = 94.41 (3)°, γ = 61.24 (3)°, and Z = 2. The structure was solved by conventional heavy-atom techniques to a final discrepancy index of R = 0.046 for 6054 independent observed reflections. The rhodacarborane anion is pseudooctahedral about the rhodium atom, and the phosphonium cation is near the rhodium-bound bromine atoms with Br?H distances of 3.06 (6) and 2.70 (6) A?. It was suggested on the basis of NMR spectral data and solubility properties that ion pairing may also be significant for [HPPh3][3] in solution. It was found that K[18-crown-6][3] could be prepared in high yield from the anionic rhodacarborane K[18-crown-6] [closo-3,3-(Ph3P)2-3,1,2-RhC2B 9H11] and bromoform. The iodo analogue of 3- could be isolated as the (n-C4H9)4N+ salt, in high yield, from the reaction of closo-3-Ph3P-3,3-NO3-3,1,2-RhC2B 9H11, (n-C4H9)4NI, and NaI in dichloromethane/water. The chloro analogue of complex 3 could be prepared as the [Et4N]+ salt from the reaction of the 16-electron complex [Et4N][closo-3-Ph3P-3,1,2-RhC2B 9H11] (generated in situ) with CH2Cl2 in 60% yield.

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