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Christopher C. Cummins

Researcher at Massachusetts Institute of Technology

Publications -  362
Citations -  13478

Christopher C. Cummins is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Triple bond & Reactivity (chemistry). The author has an hindex of 62, co-authored 342 publications receiving 12073 citations. Previous affiliations of Christopher C. Cummins include University of Miami & Harvard University.

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A retro Diels-Alder route to diphosphorus chemistry: molecular precursor synthesis, kinetics of P2 transfer to 1,3-dienes, and detection of P2 by molecular beam mass spectrometry.

TL;DR: A molecular beam mass spectrometry study on the thermolysis of solid P2A2 reveals the direct detection of molecular fragments of only P2 and anthracene, thus establishing a link between solution-phase P2-transfer chemistry and production of gas- phase P2 by mild thermal activation of a molecular precursor.
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Two-electron reduction of a vanadium(V) nitride by CO to release cyanate and open a coordination site.

TL;DR: It is reported that the terminal nitride complex Na[NV(N[t-Bu]Ar)(3)] (Na[1-VN], Ar = 3,5-Me(2)C(6)H(3)) reacts with CO over the course of 24 h to generate V(N-Bu) ( 1-V) and sodium cyanate in an isolated yield of 77%.
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Reactions of Organic Nitriles with a Three-Coordinate Molybdenum(III) Complex and with a Related Molybdaziridine-Hydride

TL;DR: In this article, the sterically hindered RCN with Me2NCN was used to give the diiminato product analogous to the one mentioned for the tert-butyl system, where molybdaziridine-hydride 2 has provided access to the threecoordinate Mo(N[i-Pr]Ar)3 (3) moiety.
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P2 Addition to Terminal Phosphide M≡P Triple Bonds: A Rational Synthesis of cyclo-P3 Complexes

TL;DR: The rate constants for the fragmentation of 1 and 1-W(CO)5 were unchanged in the presence of the terminal phosphide 3-Mo, supporting the hypothesis that molecular P2 and (P2)W( CO)5, respectively, are reactive intermediates.