Steven P. Cummings
Purdue University
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Featured researches published by Steven P. Cummings.
Journal of the American Chemical Society | 2014
Zhi Cao; Bin Xi; Diane S. Jodoin; Lei Zhang; Steven P. Cummings; Yang Gao; Sarah F. Tyler; Phillip E. Fanwick; Robert J. Crutchley; Tong Ren
Reported herein is a series of Ru2(Xap)4 capped polyyn-diyl compounds, where Xap is either 2-anilinopyridinate (ap) or its aniline substituted derivatives. Symmetric [Ru2(Xap)4](μ-C4k)[Ru2(Xap)4] (compounds 4ka (X = 3-isobutoxy) and 4kc (X = 3,5-dimethoxy) with k = 2, 3, 4, and 5) was obtained from the Glaser coupling reaction of Ru2(Xap)4(C2kH). Unsymmetric [Ru2(Xap)4](μ-C(4k+2))[Ru2(ap)4] (compounds 4k+2b with k = 2, 3, and 4) were prepared from the Glaser coupling reaction between Ru2(Xap)4(C(2k+2)H) and Ru2(ap)4(C2kH). X-ray diffraction study of compound 12c revealed both the sigmoidal topology of the polyyn-diyl bridge and the fine structural detail about the Ru2 cores. Cyclic and differential pulse voltammetric (CV and DPV) measurements and spectroelectrochemical studies revealed that (i) the reduced monoanions [Ru2-C2m-Ru2](-1) (m = 4-8) belong to the Robin-Day class II mixed valent ions and (ii) the electronic coupling between Ru2 termini depends on the length of the polyyn-diyl bridge with an attenuation constant (γ) between 0.12 and 0.15 Å(-1). In addition, spin-unrestricted DFT calculations provide insight about the nature of orbitals that mediate the long distance electronic coupling.
Journal of the American Chemical Society | 2016
Steven P. Cummings; Thanh-Ngoc Le; Gilberto E. Fernandez; Lorenzo G. Quiambao; Benjamin J. Stokes
There are few examples of catalytic transfer hydrogenations of simple alkenes and alkynes that use water as a stoichiometric H or D atom donor. We have found that diboron reagents efficiently mediate the transfer of H or D atoms from water directly onto unsaturated C-C bonds using a palladium catalyst. This reaction is conducted on a broad variety of alkenes and alkynes at ambient temperature, and boric acid is the sole byproduct. Mechanistic experiments suggest that this reaction is made possible by a hydrogen atom transfer from water that generates a Pd-hydride intermediate. Importantly, complete deuterium incorporation from stoichiometric D2O has also been achieved.
Coordination Chemistry Reviews | 2011
Steven P. Cummings; Julia Savchenko; Tong Ren
Organometallics | 2013
Steven P. Cummings; Julia Savchenko; Phillip E. Fanwick; Anastasia Kharlamova; Tong Ren
Organometallics | 2010
Steven P. Cummings; Zhi Cao; Carl W. Liskey; Alex R. Geanes; Phillip E. Fanwick; Kerry M. Hassell; Tong Ren
Inorganic Chemistry | 2012
Steven P. Cummings; Zhi Cao; Phillip E. Fanwick; Anastasia Kharlamova; Tong Ren
Langmuir | 2014
Sujitra J. Pookpanratana; Iulia Savchenko; Sean N. Natoli; Steven P. Cummings; Lee J. Richter; Joseph W. F. Robertson; Curt A. Richter; Tong Ren
Journal of Organometallic Chemistry | 2011
Steven P. Cummings; Alex R. Geanes; Phillip E. Fanwick; Anastasia Kharlamova; Tong Ren
Langmuir | 2014
Sujitra J. Pookpanratana; Joseph W. F. Robertson; Curt A. Richter; Lee J. Richter; Julia Savchenko; Steven P. Cummings; Tong Ren
Organometallics | 2013
Julia Savchenko; Zhi Cao; Sean N. Natoli; Steven P. Cummings; Boone M. Prentice; Phillip E. Fanwick; Tong Ren