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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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Second-Coordination-Sphere Assisted Selective Colorimetric Turn-on Fluoride Sensing by a Mono-Metallic Co(II) Hexacarboxamide Cryptand Complex.
TL;DR: Complex 1 represents a unique example of a fluoride sensor wherein selective F- binding takes place directly at a transition-metal center and induces a color change based upon metal-centered transitions.
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Triatomic EP2 triangles (E=Ge, Sn, Pb) as mu2:eta3,eta3-bridging ligands.
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The titanium tris-anilide cation [Ti(N[(t)Bu]Ar)3](+) stabilized as its perfluoro-tetra-phenylborate salt: structural characterization and synthesis in connection with redox activity of 4,4'-bipyridine dititanium complexes.
TL;DR: It was revealed that the aromaticity of the 4,4'-bipyridine ligand, that had been disrupted upon reduction, had been regained and should be considered as a potential intermediate in the plethora of reactions wherein Ti(N[(t)Bu]Ar)3 has been shown to effect the reduction of substrates including halogenated organic molecules, carbonyl compounds, organic nitriles, and metal complexes.
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Functionalization reactions characteristic of a robust bicyclic diphosphane framework.
TL;DR: Computational studies indicate that the oxygen-atom transfer reactions involve penta-coordinated phosphorus intermediates that have four-membered {PONC} cycles.
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Investigating CN– Cleavage by Three-coordinate M[N(R)Ar] 3 Complexes
TL;DR: In this article, the authors examined the resistance of three-coordinate Mo[N(tBu)Ar]3 to C-N bond cleavage in a mixed-metal [H2N]3Re+/CN+/W[NH2]3 system and showed that the final cleavage step is endothermic by at least 90 kJ mol−1 when symmetry constraints are relaxed.