Nick J. Mosey

Affiliations: 
Queen's University, Kingston, ON, Canada 
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"Nick Mosey"
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Manzhos S, Carrington T, Laverdure L, et al. (2015) Computing the Anharmonic Vibrational Spectrum of UF6 in 15 Dimensions with an Optimized Basis Set and Rectangular Collocation. The Journal of Physical Chemistry. A. 119: 9557-67
Kochhar GS, Heverly-Coulson GS, Mosey NJ. (2015) Theoretical Approaches for Understanding the Interplay Between Stress and Chemical Reactivity. Topics in Current Chemistry. 369: 37-96
Wu N, Melan CF, Stevenson KA, et al. (2015) Systematic study of the synthesis and coordination of 2-(1,2,3-triazol-4-yl)-pyridine to Fe(ii), Ni(ii) and Zn(ii); ion-induced folding into helicates, mesocates and larger architectures, and application to magnetism and self-selection. Dalton Transactions (Cambridge, England : 2003)
Thompson M, Carkner C, Mosey NJ, et al. (2015) Tuning the mesomorphic properties of phenoxy-terminated smectic liquid crystals: the effect of fluoro substitution. Soft Matter. 11: 3860-8
Whyte SA, Mosey NJ. (2015) Behavior of two-dimensional hydrogen-bonded networks under shear conditions: A first-principles molecular dynamics study Journal of Physical Chemistry C. 119: 350-364
Ang MTC, Phan L, Alshamrani AK, et al. (2015) Contrasting Reactivity of CS2 with Cyclic vs. Acyclic Amidines European Journal of Organic Chemistry. 2015: 7334-7343
Crudden CM, Horton JH, Ebralidze II, et al. (2014) Ultra stable self-assembled monolayers of N-heterocyclic carbenes on gold. Nature Chemistry. 6: 409-14
Thompson M, Carkner C, Bailey A, et al. (2014) Tuning the mesogenic properties of 5-alkoxy-2-(4-alkoxyphenyl)pyrimidine liquid crystals: the effect of a phenoxy end-group in two sterically equivalent series Liquid Crystals. 41: 1246-1260
Crudden CM, Horton JH, Ebralidze II, et al. (2014) Ultra stable self-assembled monolayers of N-heterocyclic carbenes on gold Nature Chemistry. 6: 409-414
Maxwell CI, Neverov AA, Mosey NJ, et al. (2014) Density functional theory study of methoxide promoted and Zn (II)-complexed methoxide promoted cleavages of aryl- and alkyl acetates in methanol. Transition from concerted to stepwise processes as a function of leaving group ability Journal of Physical Organic Chemistry. 27: 419-429
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