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1,1':2.2'-bis-μ-phenylphosphino-bis[1,2-dicarba-closo-dodecaborane(12)] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97999-96-7

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97999-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97999-96-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,9,9 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 97999-96:
(7*9)+(6*7)+(5*9)+(4*9)+(3*9)+(2*9)+(1*6)=237
237 % 10 = 7
So 97999-96-7 is a valid CAS Registry Number.

97999-96-7Downstream Products

97999-96-7Relevant academic research and scientific papers

Procedure for the degradation of 1,2-(PR2)2-1,2-dicarba-closo-dodecaborane(12) and 1-(PR2)-2-R'-1,2-dicarba-closo-dodecaborane(12)

Teixidor, Francesc,Vinnas, Clara,Abad, M. Mar,Nunnez, Rosario,Kivekaes, Raikko,Sillanpaea, Reijo

, p. 193 - 204 (1995)

Monophosphines and bisphosphines bearing anionic groups derived from the7,8-dicarba-nido-undecaborate unit, such as [7-PR2-8-Me-7,8-C2B9H10](-) and [7,8-(PR2)2-7,8-C2B9H10](-) (R = phenyl, ethyl, isopropyl or ethoxy ), were synthesized from closo-carborane precursors 1-PR2-2-Me-1,2-C2B10H10 and 1,2-(PR2)2-1,2-C2B10H10, respectively. In general, the C(c)-P bond in the closo species is very susceptible degradation reactions, producing C(c)-P cleavage and yielding the [7,8-C2B9H10]2(-) anion. Good degradation conditions which retain the C(c)-P found are toluene with a carborane-to-piperidine ratio of 1:50 and ethanol with carborane-to-piperidine ratio of 1:10. The aryl phosphines keep the C(c)-P bond best and produce the highest yields. Phosphites also retain the C(c)-P bond, but the phosphorus becomes positive and produces a zwitterionic species. Alkylphosphines are intermediate, depending on the bulk and nature of the R group in the -PR2 unit. The crystal structure of [NMe4][7,8-(PPh2)2-7,8-C2B9H10].CH3CH2OH is described.

Chemistry of decaborane-phosphorus compounds. IV. Monomeric, oligomeric, and cyclic phosphinocarboranes

Alexander, Roy P.,Schroeder, Hansjuergen

, p. 1107 - 1110 (2008/10/08)

Dilithiocarborane, B10H10C2Li2, was allowed to react with chlorophosphines containing one, two, and three chlorine atoms. (C6H5)2PCl and C6H5PCl2 gave the expected disubstituted compounds, B10H10C2[P(C6H5) 2]2 and B10H10C2(C6H 5P·Cl)2, respectively. B10H10C2Li2 and PCl3, however, formed a compound having two phosphorus atoms and two carborane nuclei in a six-membered ring. This unique ring system also arose from the reaction of B10H10C2Li2 with B10H10C2(C6H 5P·Cl)2. Subsequent reactions of such molecules with ammonia and NaN3 are described. The cyclic bis-azide, (B10H10C2P·N3)2. and p-[(C6H5)2P]2C6H 4 reacted to form a PNP bonded oligomer.

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