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[7,7-(PMe2Ph)2-nido-7-PtB10H12] is a complex organometallic compound, featuring a platinum (Pt) atom at its center, surrounded by a nido-decaborane (B10H12) ligand and two phosphine ligands, specifically bis(dimethylphenyl)phosphine (PMe2Ph). The nido-decaborane ligand is a polyhedral borane cluster with a vacant vertex, providing a unique electronic and steric environment for the central platinum atom. [7,7-(PMe2Ph)2-nido-7-PtB10H12] is of interest in the field of inorganic chemistry, particularly for its potential applications in catalysis and as a model for understanding the bonding and reactivity of transition metal complexes with borane ligands. The presence of the phosphine ligands further modulates the electronic properties and reactivity of the platinum center, making [7,7-(PMe2Ph)2-nido-7-PtB10H12] a valuable compound for studying the influence of different ligands on the chemistry of metal-borane complexes.

75309-24-9

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75309-24-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75309-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,0 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75309-24:
(7*7)+(6*5)+(5*3)+(4*0)+(3*9)+(2*2)+(1*4)=129
129 % 10 = 9
So 75309-24-9 is a valid CAS Registry Number.

75309-24-9Downstream Products

75309-24-9Relevant academic research and scientific papers

Polyhedral platinaborane chemistry. Interaction of PMe2Ph with [(PMe2Ph)2PtB10H12]

Bould, Jonathan,Cisarova, Ivana,Kennedy, John D.

, p. 2691 - 2696 (2012)

In solution, [(PMe2Ph)2PtB10H 12] (1) and PMe2Ph exist in dynamic equilibrium with [(PMe2Ph)3PtB10H12] (2). The activation energy for the dynamic process, δG≠, is ca. 63 kJ mol-1 at +17 °C, with δS being ca. 335 J mol-1 deg-1 and δH ca. 105 kJ mol-1 for the equilibrium. At low temperatures a rocking fluxionality of the {Pt(PMe2Ph) 3} unit versus the {η4-B10H12} unit in 2 becomes apparent, with an activation energy δG++ ≠ of ca. 28 kJ mol-1 at ca. -105 °C. Compound 2 is characterized by NMR spectroscopy and by a single-crystal X-ray diffraction analysis, for which the results suggest that, in contrast to the common view, the extra electron pair gained by the metal-atom center in going from 1 to 2 does not disrupt the cluster electron count proper nor the observed nido electronic structure and geometry.

The Reactions of arachno-Decaboranyl Complexes L2B10H12(L= Two-electron Donor Ligand) with some Platinum(II) Compounds; Nuclear Magnetic Resonance Studies and the Crystal and Molecular Structure of

Crook, Janet E.,Greenwood, Norman N.,Kennedy, John D.,McDonald, Walter S.

, p. 2487 - 2496 (2007/10/02)

The reactions of arachno-6,9-(SMe2)2B10H12 and of arachno-6,9-(MeCN)2B10H12 with the complex cis- give moderate yields of the nido-platinaundecaborane which has been characterised by single-crystal X-ray diffraction analysis.Analogous reactions with the dimeric species 2> (R3 = Me3-nPhn'n = 0,1 or 2), by contrast, give the nido-platinaundecaboranes which have been characterized by single-and multiple-resonance n.m.r. spectroscopy.Additional products of the reactions include the arachno nine-vertex species 4-(MeCN)B9H13 and 4-(SMe2)B9H13.

The Chemistry of Isomers of Icosaborane(26), B20H26: Synthesis and Nuclear Magnetic Resonance Study of Various Isomers of Platinahenicosaboranes and Diplatinadocosaboranes, and X-Ray Crystal and Molecular Structures of 7,7-Bis(dimethylphenylphosphine)-nido-7-platinaundecaborane and 4-...

Boocock, Simon K.,Greenwood, Norman N.,Kennedy, John D.,McDonald, Walter S.,Staves, John

, p. 2573 - 2584 (2007/10/02)

An improved synthesis of the known compound has been developed by deprotonation of B10H14 with NNN'N'-tetramethylnaphthalene-1,8-diamine followed by treatment with cis-.This reaction has been applied to the 2,2',2,6', and 1,5'isomers of (B10H13)2 to prepare various isomeric platinahenicosaborane clusters which differ either in the position of the conjuncto-linkage or the site of the platinum atom in the cluster.Appropriate modification of the reaction stoicheiometry in the case of 2,2'-(B10H13)2 led to the isolation of cisoid and transoid diplatinadocosaboranes 2>.The X-ray crystal structure of showed it to contain a platinaundecaborane cluster in which the tetrahapto B10H12 group is twisted by ca. 20 deg with respect to the PtP2 plane.Similarly, the molecular structure of the isomer of 4-B10H11-B10H13)> obtained from 2,2'-(B10H13)2 is distorted by a twist of ca. 8 deg.A detailed n.m.r. study of a number of these clusters has been made, using the resonances of 1H, 11B, 31P, and 195Pt.In addition to permitting structural assignments, the data reveal a novel mutual pseudo-rotation of the η4-B10H11X group (X=H or B10H13) and the (PMe2Ph)2 grouping about the central Pt atom.For the two sets of 1H- methyl resonances at 100 MHz coalesce at 71.5 deg C with an implied activation energy ΔG% of 79 +/- 5 kJ mol-1 for the fluxional process.Similar activation energies were deduced for the various isomers of .

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