Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Schuyler P. Lockwood"'
Publikováno v:
The Journal of Physical Chemistry A. 125:7425-7436
We use photofragment ion imaging and ab initio calculations to determine the bond strength and photodissociation dynamics of the nickel oxide (NiO+) and nickel sulfide (NiS+) cations. NiO+ photodissociates broadly from 20350 to 32000 cm-1, forming gr
Publikováno v:
The journal of physical chemistry. A. 125(34)
We use photofragment ion imaging and
Autor:
Schuyler P. Lockwood, Ricardo B. Metz
Publikováno v:
Proceedings of the 2021 International Symposium on Molecular Spectroscopy.
Publikováno v:
The Journal of Physical Chemistry A. 122:7160-7170
An analysis of the 1:1 complex of furan and water is presented. In this study, computation and matrix isolation FTIR were used to determine stable complexes of furan:water. Density functional theory and Moller–Plesset second-order, perturbation the
Publikováno v:
The journal of physical chemistry. A. 122(36)
An analysis of the 1:1 complex of furan and water is presented. In this study, computation and matrix isolation FTIR were used to determine stable complexes of furan:water. Density functional theory and Møller-Plesset second-order, perturbation theo
Publikováno v:
Proceedings of the 73rd International Symposium on Molecular Spectroscopy.
Publikováno v:
The Journal of chemical physics. 148(21)
A combination of photodissociation spectroscopy, ion imaging, and high-level theory is employed to refine the bond strength of the aluminum dimer cation (Al
Autor:
Kristin M. Slade, Schuyler P. Lockwood, Micaela A. LoConte, David J. Slade, Bridget E. Logan, Dominique I. Hargreaves, Michael J. Conroy, Samuel H. Schneider, Erin E. McLaughlin
Publikováno v:
Biochemistry. 54:5898-5906
To understand the consequences of macromolecular crowding, studies have largely employed in vitro experiments with synthetic polymers assumed to be both pure and "inert". These polymers alter enzyme kinetics by excluding volume that would otherwise b
Publikováno v:
The Journal of Chemical Physics. 148:214308
A combination of photodissociation spectroscopy, ion imaging, and high-level theory is employed to refine the bond strength of the aluminum dimer cation (Al2+) and elucidate the electronic structure and photodissociation dynamics between 38 500 and 4