Search Results

Search criteria:

You may also wish to search for items by Poutsma.

11 matching references were found.

Kuntz, A.F.; Boynton, A.W.; David, G.A.; Colyer, K.E.; Poutsma, J.C., The Proton Affinity of Proline Analogues Using the Kinetic Method with Full Entropy Correction, J. Am. Soc. Mass Spectrom., 2002, 13, 72. [all data]

Poutsma, J.C.; Andriole, E.J.; Sissung, T.; Morton, T.H., cis-1,5-Diaminocyclooctane: The most basic gaseous primary amine?, Chem. Communications, 2003, 2040. [all data]

Schroeder, O.E.; Andriole, E.J.; Carver, K.L.; Colyer, K.E.; Poutsma, J.C., Proton affinity of lysine homologues from the extended kinetic method, J. Phys. Chem. A, 2004, 108, 326. [all data]

Wind, J.J.; Papp, L.; Happel, M.; Hahn, K.; Andriole, E.J.; Poutsma, J.C., Proton Affinity of beta-Oxalylaminoalanine (BOAA): Incorporation of Direct Entropy Correction into the Single-Reference Kinetic Method, J. Am. Soc. Mass Spectrom., 2005, 16, 1151. [all data]

Poutsma, J.C.; Schroeder, O.E.; Squires, R.R., Experimental chloride ion affinities and theoretical predictions for the absolute heats of formation of SiCl2 and SiClF, Chem. Phys. Lett., 2004, 389, 4-6, 433-437, https://doi.org/10.1016/j.cplett.2004.03.137 . [all data]

Webb, I.K.; Muetterties, C.E.; Platner, C.B.; Poutsma, J.C., Gas-phase acidities of lysine homologues and proline analogs from the extended kinetic method, Int. J. Mass Spectrom., 2012, 316, 126-132, https://doi.org/10.1016/j.ijms.2011.12.017 . [all data]

Jones, C.M.; Bernier, M.; Carson, E.; Colyer, K.E.; Metz, R.; Pawlow, A.; Wischow, E.D.; Webb, I.; Andriole, E.J.; Poutsma, J.C., Gas-phase Acities of the 20 Protein Amino Acids, Int. J. Mass Spectrom., 2007, 267, 1-3, 54-62, https://doi.org/10.1016/j.ijms.2007.02.018 . [all data]

Poutsma, J.C.; Nash, J.J.; Paulino, J.A.; Squires, R.R., Absolute Heats of Formation of Phenylcarbene and Vinylcarbene, J. Am. Chem. Soc., 1997, 119, 20, 4686, https://doi.org/10.1021/ja963918s . [all data]

Tian, Z.X.; Pawlow, A.; Poutsma, J.C.; Kass, S.R., Are carboxyl groups the most acidic sites in amino acids? Gas-phase acidity, H/D exchange experiments, and computations on cysteine and its conjugate base, J. Am. Chem. Soc., 2007, 129, 17, 5403-5407, https://doi.org/10.1021/ja0666194 . [all data]

Poutsma, J.C.; Paulino, J.A.; Squires, R.R., Absolute Heats of Formation of CHCl, CHF, and CClF. A Gas-Phase Experimental and G2 Theoretical Study., J. Phys. Chem. A, 1997, 101, 29, 5327, https://doi.org/10.1021/jp970778f . [all data]

Poutsma, J.C.; Upshaw, S.D.; Squires, R.R.; Wenthold, P.G., Absolute heat of formation and singlet-triplet splitting for HCCN, J. Phys. Chem. A, 2002, 106, 6, 1067-1073, https://doi.org/10.1021/jp013653q . [all data]