Serge Ruccolo

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2016- Chemistry Harvard University, Cambridge, MA, United States 
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"Serge Ruccolo"
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Sun R, Qin Y, Ruccolo S, et al. (2018) Elucidation of a Redox-Mediated Reaction Cycle for Nickel-Catalyzed Cross Coupling. Journal of the American Chemical Society
Ruccolo S, Qin Y, Schnedermann C, et al. (2018) General Strategy for Improving the Quantum Efficiency of Photoredox Hydroamidation Catalysis. Journal of the American Chemical Society
Ruccolo S, Rauch M, Parkin G. (2017) Tris[(1-isopropylbenzimidazol-2-yl)dimethylsilyl]methyl metal complexes, [Tism]M: a new class of metallacarbatranes, isomerization to a tris(N-heterocyclic carbene) derivative, and evidence for an inverted ligand field. Chemical Science. 8: 4465-4474
Rauch M, Ruccolo S, Parkin G. (2017) Synthesis, Structure, and Reactivity of a Terminal Magnesium Hydride Compound with a Carbatrane Motif, [Tism(Pr(i)Benz)]MgH: A Multifunctional Catalyst for Hydrosilylation and Hydroboration. Journal of the American Chemical Society
Rauch M, Ruccolo S, Mester JP, et al. (2016) Synthesis, structure and reactivity of a terminal magnesium fluoride compound, [Tp]MgF: hydrogen bonding, halogen bonding and C-F bond formation. Chemical Science. 7: 142-149
Chakrabarti N, Ruccolo S, Parkin G. (2016) Cadmium Compounds with an [N3C] Atrane Motif: Evidence for the Generation of a Cadmium Hydride Species. Inorganic Chemistry. 55: 12105-12109
Ruccolo S, Sattler W, Rong Y, et al. (2016) Modulation of Zn-C Bond Lengths Induced by Ligand Architecture in Zinc Carbatrane Compounds. Journal of the American Chemical Society
Li G, Estes DP, Norton JR, et al. (2014) Dihydrogen activation by cobaloximes with various axial ligands. Inorganic Chemistry. 53: 10743-7
Sattler W, Ruccolo S, Parkin G. (2013) Synthesis, structure, and reactivity of a terminal organozinc fluoride compound: hydrogen bonding, halogen bonding, and donor-acceptor interactions. Journal of the American Chemical Society. 135: 18714-7
Eberhart MS, Norton JR, Zuzek A, et al. (2013) Electron transfer from hexameric copper hydrides. Journal of the American Chemical Society. 135: 17262-5
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