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The chemical compound "(Rh(P(CH3)2(C6H5))C2B9H11)2" is a complex organometallic molecule consisting of two identical units. Each unit features a rhodium (Rh) atom at the center, coordinated to two phosphorus (P) atoms from triphenylphosphine ligands (P(CH3)2(C6H5)), which are organic compounds with a phosphorus atom bonded to three phenyl groups and two methyl groups. Additionally, the rhodium is bonded to a dicarbollide anion (C2B9H11), which is a polyhedral anion composed of two carbon atoms and nine boron atoms, with eleven hydrogen atoms attached. The entire structure is symmetrical, with two of these units linked together, forming a dimeric complex. (Rh(P(CH3)2(C6H5))C2B9H11)2 is of interest in the field of organometallic chemistry and catalysis due to its unique structure and potential applications in various chemical transformations.

94294-05-0

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94294-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94294-05-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,2,9 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94294-05:
(7*9)+(6*4)+(5*2)+(4*9)+(3*4)+(2*0)+(1*5)=150
150 % 10 = 0
So 94294-05-0 is a valid CAS Registry Number.

94294-05-0Downstream Products

94294-05-0Relevant academic research and scientific papers

Synthesis, Stuctural Characterization, and Stereospecificity in the Formation of Bimetallic Rhodacarborane Clusters Containing Rh-H-B Bridge Interactions

Behnken, Paul E.,Marder, Tood B.,Baker, R. Thomas,Knobler, Carolyn B.,Thompson, Michael R.,Hawthorne, M. Frederick

, p. 932 - 940 (2007/10/02)

Reactions of (COD=η4-1,5-cyclooctadiene; R=Ph; Et; Ph, Me) with resulted in the formation of bimetallic rhodacarborane clusters containing Rh-Rh bonds supported by Rh-H-B interactions. 2 (2) is formed stereospecifically as the nature of the Rh-H-B interactions determines a specific stereoisomer and of the six possible only the structure of 2 is observed.The synthesis, characterization, and X-ray structure determinations of analogues of 2 containing differing phosphine ligands demonstrate this stereospecificity to be of thermodynamic origin, arising from polyhedral repulsions on adjacent carborane ligands.The characterization of (8) as well as experiments observing the formation of 2 result in a general mechanism for their formation involving hydrogenation of the COD ligand to cyclooctene via phosphine ligand disproportionation. 2 (2) crystallizes in the triclinic space group P1 with unit cell parameters a=11.118(2) Angstroem, b=13.456(3) Angstroem, c=18.390(3) Angstroem, α=93.09(2) deg, β=76.22(1) deg, γ=76.90(2) deg, Z=2. 2 (3) crystallizes in the monoclinic space group P21/c with unit cell parameters a=11.153(6) Angstroem, b=15.228(9) Angstroem, c=18.844(10) Angstroem, β=91.83(2) deg, Z=4. 2 (5) crystallizes in the monoclinic space group P21/c with unit cell parameters a=18.035(6) Angstroem, b=13.156(4) Angstroem, c=26.905(8) Angstroem, β=113.34(2) deg, Z=4. (8) crystallizes in the monoclinic space group P21/n with unit cell parameters a=14.043(7) Angstroem, b=32.638(13) Angstroem, c=10.059(4) Angstroem, β=98.98(3) deg, Z=4.

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