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(methoxycarbonylmethyl)tetracarbonyltriphenylphosphinemanganese is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77438-16-5

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77438-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77438-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,3 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 77438-16:
(7*7)+(6*7)+(5*4)+(4*3)+(3*8)+(2*1)+(1*6)=155
155 % 10 = 5
So 77438-16-5 is a valid CAS Registry Number.

77438-16-5Downstream Products

77438-16-5Relevant academic research and scientific papers

Transformations of group 7 carbonyl complexes: Possible intermediates in a homogeneous syngas conversion scheme

Elowe, Paul R.,West, Nathan M.,Labinger, Jay A.,Bercaw, John E.

, p. 6218 - 6227 (2010/01/29)

A variety of C-H and C-C bond forming reactions of group 7 carbonyl complexes have been studied as potential steps in a homogeneously catalyzed conversion of syngas to C2+ compounds. The metal formyl complexes M(CO)3(PPh3)2(CHO) (M = Mn, Re) are substantially stabilized by coordination of boranes BX3 (X = F, C6F5) in the form of novel boroxycarbene complexes M(CO)3- (PPh3)2(CHOBX3), but these boron-stabilized carbenes do not react with hydride sources to undergo further reduction to metal alkyls. The related manganese methoxycarbene cations [Mn(CO)5-x(PPh3)x(CHOMe)]+ (x = 1 or 2), obtained by methylation of the formyls, do react with hydrides to form methoxymethyl complexes, which undergo further migratory insertion under an atmosphere of CO. The resulting acyls, cis- and trans-Mn(PPh3)(CO) 4(C(O)CH2OMe), can be alkylated to form the cationic carbene complex [Mn(PPh3)(CO)4(C(OR)CH2OMe)] +, which undergoes a 1,2 hydride shift to form 1,2-dialkoxyethylene, which is displaced from the metal, releasing triflate or diethyl ether adducts of [Mn(PPh3)(CO)4]+. The acyl can also be protonated with HOTf to form a hydroxycarbene complex, which rearranges to Mn(PPh3)(CO)4(CH2COOMe) and is protonolyzed to yield methyl acetate and [Mn(PPh3)(CO)4]+; addition of L (L = PPh3, CO) to the manganese cation regenerates [Mn(PPh3)(CO)4(L)]+. Since the original formyl complex can be obtained by the reaction of [Mn(PPh3)(CO) 5]+ with [PtH(dmpe)2]+, which in turn can be generated from H2, this set of transformations amounts to a stoichiometric cycle for selectively converting H2 and CO into a C2 compound under mild conditions.

DARSTELLUNG UND EIGENSCHAFTEN VON ACETONYL-, PHENACYL- UND ACETOMETHOXY-MANGANCARBONYLVERBINDUNGEN. DIE KRISTALLSTRUKTUR VON ACETONYLTETRACARBONYLTRIPHENYLPHOSPHINMANGAN

Engelbrecht, Juergen,Greiser, Thomas,Weiss, Erwin

, p. 79 - 92 (2007/10/02)

Several oxoalkylpentacarbonylmanganese compounds RC(O)CH2Mn(CO)5 (R = Me, Ph, MeO) have been synthesized and investigated (IR, 1H NMR, mass spectra).They are thermo- and photo-labile and can be stabilized by triphenylphosphine substitution.Thus acetonylte

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