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Geeson, M. B.; R´ıos, P.; Transue, W. J.; Cummins, C. C., Orthophosphate and sulfate utilization for C–E (E = P, S) bond formation via trichlorosilyl phosphide and sulfide anions. J. Am. Chem. Soc.2019, 141, 0000–0000. URL https://doi.org/10.1021/jacs.9b01475.
Szkop, K. M.; Geeson, M. B.; Stephan, D. W.; Cummins, C. C., Synthesis of acyl(chloro)phosphines enabled by phosphinidene transfer. Chem. Sci. 2019, 10, 3627–3631. URL https://doi.org/10.1039%2Fc8sc05657a.
Shepard, S.; Cummins, C. C., Functionalization of intact trimetaphosphate: A triphosphorylating reagent for C, N, and O nucleophiles. J. Am. Chem. Soc. 2019, 141, 1852–1856. URL https://doi.org/10.1021/jacs.8b12204.
Transue, W. J.; Nava, M.; Terban, M. W.; Yang, J.; Greenberg, M. W.; Wu, G.; Foreman, E. S.;Mustoe, C. L.; Kennepohl, P.; Owen, J. S.; Billinge, S. J. L.; Kulik, H. J.; Cummins, C. C., Anthracene as a launchpad for a phosphinidene sulfide and for generation of a phosphorus-sulfur material having the composition P2S, a vulcanized red phosphorus that is yellow. J. Am. Chem. Soc. 2019, 141,431–440. URL https://doi.org/10.1021%2Fjacs.8b10775.
Transue, W. J.; Yang, J.; Nava, M.; Sergeyev, I. V.; Barnum, T. J.; McCarthy, M. C.; Cummins, C. C.,Synthetic and spectroscopic investigations enabled by modular synthesis of molecular phosphaalkyne precursors. J. Am. Chem. Soc. 2018, 140, 17985–17991. URL https://doi.org/10.1021%2Fjacs.8b09845.
Paparo, A.; Silvia, J. S.; Spaniol, T. P.; Okuda, J.; Cummins, C. C., Countercation effect on CO2 binding to oxo titanate with bulky anilide ligands. Chem.–Eur. J. 2018, 24, 17072–17079. URL https://doi.org/10.1002%2Fchem.201803265.
qin Yuan, Q.; Yang, Z.; zhong Li, R.; Transue, W. J.; peng Li, Z.; Jiang, L.; Govind, N.; Cummins,C. C.; Wang, X.-B., Magnetic-bottle and velocity-map imaging photoelectron spectroscopy of APS−(A=C14H10 or anthracene): Electron structure, spin-orbit coupling of APS•, and dipole-bound state of APS−. Chin. J. Chem. Phys. 2018, 31, 463–470. URL https://doi.org/10.1063%2F1674-0068%2F31%2Fcjcp1805114.
Ghosh, S. K.; Cummins, C. C.; Gladysz, J. A., A direct route from white phosphorus and fluorous alkyl and aryl iodides to the corresponding trialkyl- and triarylphosphines. Org. Chem. Front. 2018.URL https://doi.org/10.1039%2Fc8qo00943k.
Joost, M.; Nava, M.; Transue, W. J.; Martin-Drumel, M.-A.; McCarthy, M. C.; Patterson, D.; Cummins, C. C., Sulfur monoxide thermal release from an anthracene-based precursor, spectroscopic identification, and transfer reactivity. Proc. Natl. Acad. Sci. U. S. A. 2018, 115, 5866–5871. URL https://doi.org/10.1073%2Fpnas.1804035115.
Geeson, M. B.; Cummins, C. C., Phosphoric acid as a precursor to chemicals traditionally synthesized from white phosphorus. Science 2018, 359, 1383–1385. URL https://doi.org/10.1126%2Fscience.aar6620.
Stauber, J. M.; Zhang, S.; Gvozdik, N.; Jiang, Y.; Avena, L.; Stevenson, K. J.; Cummins, C. C.,Cobalt and vanadium trimetaphosphate polyanions: Synthesis, characterization, and electrochemical evaluation for non-aqueous redox-flow battery applications. J. Am. Chem. Soc. 2018, 140, 538–541.
Joost, M.; Transue, W. J.; Cummins, C. C., Diazomethane umpolung atop anthracene: an electrophilic methylene transfer reagent. Chem. Sci. 2018, 9, 1540–1543. URL https://doi.org/10.1039%2Fc7sc04506a.
Knopf, I.; Courtemanche, M.-A.; Cummins, C. C., Cobalt complexes supported by cis-macrocyclic diphosphines: Synthesis, reactivity, and activity toward coupling carbon dioxide and ethylene.Organometallics 2017, 36, 4834–4843. URL https://doi.org/10.1021%2Facs.organomet.7b00734.
Joost, M.; Nava, M.; Transue, W. J.; Cummins, C. C., An exploding N-isocyanide reagent formally composed of anthracene, dinitrogen and a carbon atom. Chem. Commun. 2017, 53, 11500–11503. URL https://doi.org/10.1039%2Fc7cc06516g.
Joost, M.; Transue, W. J.; Cummins, C. C., Terminal tungsten pnictide complex formation through pnictaethynolate decarbonylation. Chem. Commun. 2017, 53, 10731–10733. URL https://dx.doi.org/10.1039/c7cc06841g.
Transue, W. J.; Velian, A.; Nava, M.; Garca-Iriepa, C.; Temprado, M.; Cummins, C. C., Mechanism and scope of phosphinidene transfer from dibenzo-7-phosphanorbornadiene compounds. J. Am. Chem.Soc. 2017, 139, 10822–10831. URL http://dx.doi.org/10.1021/jacs.7b05464, pMID: 28703579.
Stauber, J. M.; Alliger, G. E.; Nocera, D. G.; Cummins, C. C., Second-coordination-sphere assisted selective colorimetric turn-on fluoride sensing by a mono-metallic Co(II) hexacarboxamide cryptand complex. Inorg. Chem. 2017, 56, 7615–7619. URL http://dx.doi.org/10.1021/acs.inorgchem.7b01335, pMID: 28665117.
Zhang, S.; Nava, M. J.; Chow, G.; Lopez, N.; Wu, G.; Britt, R. D.; Nocera, D. G.; Cummins, C., On the incompatibility of lithium-O2 battery technology with CO2. Chem. Sci. 2017, 8, 6117–6122. URL http://dx.doi.org/10.1039/C7SC01230F.
Hou, G.-L.; Chen, B.; Transue, W. J.; Yang, Z.; Gr¨utzmacher, H.; Driess, M.; Cummins, C. C.; Borden,W. T.; Wang, X.-B., Spectroscopic characterization, computational investigation, and comparisons of ECX− (E = As, P, and N; X = S and O) anions. J. Am. Chem. Soc. 2017, 139, 8922–8930. URL http://dx.doi.org/10.1021/jacs.7b02984, pMID: 28589728.
Green, M. L. H.; Cummins, C. C.; Kronauge, J. F., Alan Davison. 24 March 1936 — 14 November 2015. Biographical Memoirs of Fellows of the Royal Society 2017, page rsbm20170004. URL https://doi.org/10.1098/rsbm.2017.0004.
Stauber, J. M.; Cummins, C. C., Terminal titanyl complexes of tri- and tetrametaphosphate: Synthesis,structures, and reactivity with hydrogen peroxide. Inorg. Chem. 2017, 56, 3022–3029. URL https://doi.org/10.1021%2Facs.inorgchem.6b03149.
Knopf, I.; Tofan, D.; Beetstra, D.; Al-Nezari, A.; Al-Bahily, K.; Cummins, C., A family of cismacrocyclic diphosphines: modular, stereoselective synthesis and application in catalytic CO2/ethylene coupling. Chem. Sci. 2017, 8, 4163–4168. URL http://dx.doi.org/10.1039/C6SC03614G.
Courtemanche, M.-A.; Transue, W. J.; Cummins, C. C., Phosphinidene reactivity of a transient vanadium P≡N complex. J. Am. Chem. Soc. 2016, 138, 16220–16223. URL https://doi.org/10.1021%2Fjacs.6b10545.
Nava, M.; Martin-Drumel, M.-A.; Lopez, C. A.; Crabtree, K. N.; Womack, C. C.; Nguyen, T. L.;Thorwirth, S.; Cummins, C. C.; Stanton, J. F.; McCarthy, M. C., Spontaneous and selective formation of HSNO, a crucial intermediate linking H2S and nitroso chemistries. J. Am. Chem. Soc. 2016, 138,11441–11444. URL http://dx.doi.org/10.1021/jacs.6b05886.
Hou, G.-L.; Chen, B.; Transue, W. J.; Hrovat, D. A.; Cummins, C. C.; Borden, W. T.; Wang, X.-B., A joint experimental and computational study of the negative ion photoelectron spectroscopy of the 1-phospha-2,3,4-triazolate anion, HCPN−3. J. Phys. Chem. A 2016, 120, 6228–6235. URL http://dx.doi.org/10.1021/acs.jpca.6b06343.
Stauber, J. M.; Mueller, P.; Dai, Y.; Wu, G.; Nocera, D. G.; Cummins, C. C., Multi-electron reactivity of a cofacial di-tin(II) cryptand: Partial reduction of sulfur and selenium and reversible generation of S·−3. Chem. Sci. 2016, 7, 6928–6933. URL http://dx.doi.org/10.1039/C6SC01754A.
Chakarawet, K.; Knopf, I.; Nava, M.; Jiang, Y.; Stauber, J. M.; Cummins, C. C., Crystalline metaphosphate acid salts: Synthesis in organic media, structures, hydrogen-bonding capability, and implication of superacidity. Inorg. Chem. 2016, 55, 6178–6185. URL http://dx.doi.org/10.1021/acs.inorgchem.6b00749.
Transue, W. J.; Velian, A.; Nava, M.; Martin-Drumel, M.-A.; Womack, C. C.; Jiang, J.; Hou, G.-L.;Wang, X.-B.; McCarthy, M. C.; Field, R. W.; Cummins, C. C., A molecular precursor to phosphaethyne and its application in synthesis of the aromatic 1,2,3,4-phosphatriazolate anion. J. Am. Chem. Soc.2016, 138, 6731–6734. URL http://dx.doi.org/10.1021/jacs.6b03910.
Hou, G.-L.; Chen, B.; Transue, W. J.; Hrovat, D. A.; Cummins, C. C.; Borden, W. T.; Wang, X.-B.,Negative ion photoelectron spectroscopy of P2N−3: electron affinity and electronic structures of P2N3·.Chem. Sci. 2016, 7, 4667–4675. URL http://dx.doi.org/10.1039/C5SC04667J.
Velian, A.; Cossairt, B. M.; Cummins, C. C., Assembly and stabilization of E(cyclo-P3)2 (E = Sn, Pb) as a bridging ligand spanning two triaryloxyniobium units. Dalton Trans. 2016, 45, 1891–1895. URL http://dx.doi.org/10.1039/c5dt03383g.