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[8,8,8-(H)(PMe2Ph)2-9-(pyridine)-nido-8,7-RhSB9H9] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1370735-89-9

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1370735-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1370735-89-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,0,7,3 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1370735-89:
(9*1)+(8*3)+(7*7)+(6*0)+(5*7)+(4*3)+(3*5)+(2*8)+(1*9)=169
169 % 10 = 9
So 1370735-89-9 is a valid CAS Registry Number.

1370735-89-9Downstream Products

1370735-89-9Relevant academic research and scientific papers

Modification of [8,8,8-(H)(PPh3)2-9-(Py)- Nido -8,7-RhSB9H9], Py = NC5H5, with monodentate phosphines: Reactivity and mechanistic insights

Calvo, Beatriz,Alvarez, Alvaro,Macias, Ramon,Garcia-Orduna, Pilar,Lahoz, Fernando J.,Oro, Luis A.

, p. 2986 - 2995 (2012)

The [8,8,8-(H)(PPh3)2-9-(Py)-nido-8,7-RhSB 9H9] (2)/[1,1-(PPh3)2-3-(Py)-closo- 1,2-RhSB9H8] (3) pair catalyzes the hydrogenation of olefins through nido-to-closo transformations. Substitution of the phosphine ligands can lead to an improvement of the catalytic activity of this system. Therefore, the substitutional chemistry of 2 with PMePh2, PMe 2Ph, and PMe3 has been studied, leading to the formation of [8,8,8-(H)(PPh3)(PR3)-9-(Py)-nido-8,7-RhSB 9H9], where R3 = Me2Ph (5) or Me3 (6), and [8,8,8-(H)(PR3)2-9-(Py)-nido-8,7- RhSB9H9], where R3 = MePh2 (4) or Me2Ph (7). Kinetic studies on the reaction of PMe2Ph with 2 indicate that the substitutions follow a dissociative mechanism. The thermal dehydrogenation of 5-7 affords the corresponding closo-derivatives [1,1-(L)(PPh3)-3-(Py)-closo-1,2-RhSB9H8], where L = PMe2Ph (9) or PMe3 (10), and [1,1-(L) 2-3-(Py)-closo-1,2-RhSB9H8], where L = PMe 2Ph (11) or PMe3 (12). The substitution of PPh3 by the more basic, less bulky phosphines facilitates hydrogen loss and consequent nido-to-closo transformations. The reaction of 5 and 6 with C 2H4 promotes a nido-to-closo cluster change and the consequent formation of 10 and 11 together with small amounts of C 2H4-ligated [1,1-(η2-C2H 4)(L)-3-(Py)-closo-1,2-RhSB9H8], where L = PPh3 (13) or PMe3 (15), characterized in situ by 1H NMR spectroscopy. In the reactions with ethylene, ethane is detected in situ, indicating that the olefin is hydrogenated. The reactions of 5 and 6 with CO afford the CO-ligated [1,1-(CO)(L)-3-(Py)-closo-1,2-RhSB 9H8], where L = PMe2Ph (16) or PMe3 (17). The reactivity of the new PR3-ligated nido-clusters versus H2, C2H4, and CO is not improved with the phosphines studied in this work; however, the changes found in the chemical beahavior of this system are dramatic, confirming the tailorability of these 11-vertex rhodathiaboranes and the potential optimization of their catalytic activity by the judicious choice of the exo-polyhedral ligands.

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