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Valence (chemistry)

About: Valence (chemistry) is a research topic. Over the lifetime, 24937 publications have been published within this topic receiving 645252 citations. The topic is also known as: valency.


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Journal ArticleDOI
TL;DR: In this article, reflection electron energy loss spectroscopy as a function of the electron beam incidence angle α was performed on silicene nanoribbons, and the spectra revealed the presence of two distinct loss structures attributed to transitions 1s→π∗ and 1 s→σ∗, according to their intensity dependence on α.
Abstract: Silicene nanoribbons grown on a silver (110) substrate have been studied by reflection electron energy loss spectroscopy as a function of the electron beam incidence angle α. The spectra, taken at the Si K absorption edge (1.840 keV), reveal the presence of two distinct loss structures attributed to transitions 1s→π∗ and 1s→σ∗, according to their intensity dependence on α. Such behavior, when compared to graphite, attests the sp2-like hybridization of the silicon valence orbitals in the silicene nanoribbons as is, indeed, for carbon atomic bonds of graphene.

156 citations

Journal ArticleDOI
TL;DR: The combination of equilibrium and dynamic behavior of DNA nanostars demonstrates the potential of DNA molecules in diversifying the pathways toward collective properties and self-assembled materials, beyond the range of phenomena accessible with ordinary molecular fluids.
Abstract: Colloidal particles with directional interactions are key in the realization of new colloidal materials with possibly unconventional phase behaviors. Here we exploit DNA self-assembly to produce bulk quantities of “DNA stars” with three or four sticky terminals, mimicking molecules with controlled limited valence. Solutions of such molecules exhibit a consolution curve with an upper critical point, whose temperature and concentration decrease with the valence. Upon approaching the critical point from high temperature, the intensity of the scattered light diverges with a power law, whereas the intensity time autocorrelation functions show a surprising two-step relaxation, somehow reminiscent of glassy materials. The slow relaxation time exhibits an Arrhenius behavior with no signs of criticality, demonstrating a unique scenario where the critical slowing down of the concentration fluctuations is subordinate to the large lifetime of the DNA bonds, with relevant analogies to critical dynamics in polymer solutions. The combination of equilibrium and dynamic behavior of DNA nanostars demonstrates the potential of DNA molecules in diversifying the pathways toward collective properties and self-assembled materials, beyond the range of phenomena accessible with ordinary molecular fluids.

156 citations

Journal ArticleDOI
TL;DR: In this article, relativistic and non-relativistic Hartree-Fock one-centre expansion calculations including valence s and p orbitals are reported for CuH, AgH and AuH molecules.

155 citations

Journal ArticleDOI
TL;DR: The autocorrelation function of the donor-acceptor tunneling matrix element for six Ru-azurin derivatives is computed and it is shown that for azurin, the correlation function is remarkably insensitive to tunneling pathway structure.
Abstract: We compute the autocorrelation function of the donor-acceptor tunneling matrix element for six Ru-azurin derivatives. Comparison of this decay time to the decay time of the time-dependent Franck-Condon factor {computed by Rossky and coworkers [Lockwood, D. M., Cheng, Y.-K. & Rossky, P. J. (2001) Chem. Phys. Lett. 345, 159-165]} reveals the extent to which non-Condon effects influence the electron-transfer rate. is studied as a function of donor-acceptor distance, tunneling pathway structure, tunneling energy, and temperature to explore the structural and dynamical origins of non-Condon effects. For azurin, the correlation function is remarkably insensitive to tunneling pathway structure. The decay time is only slightly shorter than it is for solvent-mediated electron transfer in small organic molecules and originates, largely, from fluctuations of valence angles rather than bond lengths.

155 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20231,521
20222,997
2021616
2020611
2019584
2018577