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WI(CO)3(NO)(P(C6H5)3) is a complex organometallic compound consisting of a tungsten (W) center, which is a transition metal. The compound features three carbonyl (CO) ligands, a nitrosyl (NO) ligand, and a triphenylphosphine (P(C6H5)3) ligand. The carbonyl ligands are neutral two-electron donors, while the nitrosyl ligand can act as a one-electron donor or acceptor, depending on its oxidation state. The triphenylphosphine ligand is a strong sigma donor, providing additional stability to the complex. WI(CO)3(NO)(P(C6H5)3) is of interest in organometallic chemistry and catalysis due to its unique electronic properties and potential applications in various chemical transformations.

43128-73-0

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43128-73-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 43128-73-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,1,2 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 43128-73:
(7*4)+(6*3)+(5*1)+(4*2)+(3*8)+(2*7)+(1*3)=100
100 % 10 = 0
So 43128-73-0 is a valid CAS Registry Number.

43128-73-0Downstream Products

43128-73-0Relevant academic research and scientific papers

Syntheses and reactions of WH(CO)2(NO)(P(C6H5)3)2 and related tungsten nitrosyl complexes

Hillhouse, Gregory L.,Haymore, Barry L.

, p. 1876 - 1885 (2008/10/08)

cis-W(CO)4(PPh3)2 (1c) or trans-W(CO)4(PR3)2 (1t) (R = C6H5, p-CH3C6H4) reacted with NOPF6 in methylene chloride to give cis,mer-[W(CO)3(NO)(PR3)2][PF6] (2-PF6); BF4- and ClO4- salts (2-BF4; 2-ClO4) were also prepared. Halide anions (X = Cl-, Br-, I-) reacted with 2 first to give mer-WX(CO)3(NO)(PPh3) (7a, X = Cl; 7b, X = Br; 7c, X = I) and PPh3, then cis,cis-WX(CO)2(NO)(PPh3)2 (6a, X = Cl; 6b, X = Br; 6c, X = I), and finally trans,trans-WX(CO)2(NO)(PPh3)2 (3a, X = F; 3b, X = Cl; 3c, X = Br; 3d, X = I). Further reaction of 3c with NOPF6 and n-Bu4NX gave WXBr(NO)2(PPh3)2 (4c, X = Br; 4f, X = F). Upon reaction with NO+, trans-Cr(CO)4(PPh3)2 gave good yields of trans-[Cr(CO)4(PPh3)2][PF6] (5), but trans-Mo(CO)4(PPh3)2 produced complex mixtures. Acetate reacted with 2 to form trans,trans-W(η1-CH3CO2)(CO) 2(NO)(PPh3)2 (8) and then trans-W(η2-CH3CO2)(CO)(NO)(PPh 3)2 (11) and CO. Dimethyldithiocarbamate reacted with 2 to form cis-W-(η2-S2CNMe2)(CO) 2(NO)(PPh3) (13) and PPh3 and then trans-W(η2-S2CNMe2)(CO)(NO)(PPh 3)2 (14). In the presence of LiBH4 and PPh3 in tetrahydrofuran, both 3c and 2 were transformed into the tungsten(0) hydride trans,trans-WH(CO)2-(NO)(PPh3)2 (15). This hydride underwent α-insertion reactions with RN3 and RN2+, forming trans-W(η2-RN3H)(CO)-(NO)(PPh3)2 (19a, R = Ph; 19b, R = To) and trans,trans-[W(RN2H)(CO)2(NO)(PPh3) 2]+ (23, R = Ph; 24, R = To), and it underwent β-insertion reactions with RNCNR, CO2, and CS2, forming trans-W(η2-RNCHNR)(CO)(NO)(PPh3)2 (21, R = To), trans,trans-W(η1-HCO2)(CO)2(NO)(PPh 3)2 (9), and trans,trans-W(η1-HCS2)(CO)2(NO)(PPh 3)2 (22). Heating the hydride with RN=NNHR and RN=CHNHR produced trans-W(η2-RN3R)(CO)(NO)(PPh3)2 (20) and 21, respectively. When allowed to react with acids (HX; X = Cl, Br, I, CH3CO2, HCO2, OClO3), 15 gave trans,trans-WX(CO)2(NO)(PPh3)2 (3b, 3c, 3d, 8, 9, 16 (X = OClO3)). The perchlorato ligand in 16 was rapidly displaced by halide and pseudohalide anions but not by CO even at 1000 psi (20-80°C).

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