A Strong Preference for a Salt-Bridge Structure in the Gas Phase:  Reactions of Deprotonated Amino Acids with Borane

2001 ◽  
Vol 123 (35) ◽  
pp. 8606-8607 ◽  
Author(s):  
Scott Gronert ◽  
Renee Huang
Keyword(s):  
Amino Acids ◽  
Gas Phase ◽  
Salt Bridge ◽  
Strong Preference ◽  
Bridge Structure ◽  
Gas Phase Reactions

Vibrational Signature of Charge Solvation vs Salt Bridge Isomers of Sodiated Amino Acids in the Gas Phase

2004 ◽  
Vol 126 (6) ◽  
pp. 1836-1842 ◽  
Author(s):  
Catherine Kapota ◽  
Joël Lemaire ◽  
Philippe Maître ◽  
Gilles Ohanessian
Keyword(s):  
Amino Acids ◽  
Gas Phase ◽  
Salt Bridge ◽  
Charge Solvation

Gas-Phase Reactions

1981 ◽  
Author(s):  
Victor N. Kondratiev ◽  
Evgeniĭ E. Nikitin
Keyword(s):  
Gas Phase ◽  
Gas Phase Reactions

Influence of Gas Mixing and Heating on Gas-Phase Reactions in GaN MOCVD Growth

2012 ◽  
Vol 1 (1) ◽  
pp. P46-P53 ◽  
Author(s):  
Ran Zuo ◽  
Haiqun Yu ◽  
Nan Xu ◽  
Xiaokun He
Keyword(s):  
Gas Phase ◽  
Gas Mixing ◽  
Gas Phase Reactions ◽  
Mocvd Growth

Gas Phase Reactions Activated by Nuclear Processes

1957 ◽  
Vol 79 (17) ◽  
pp. 4609-4616 ◽  
Author(s):  
Adon A. Gordus ◽  
John E. Willard
Keyword(s):  
Gas Phase ◽  
Gas Phase Reactions ◽  
Nuclear Processes

Nanocomposite ceramic powder production by laser-induced gas-phase reactions

1993 ◽  
Vol 168 (2) ◽  
pp. 177-181 ◽  
Author(s):  
E Borsella ◽  
S Botti ◽  
R Alexandrescu ◽  
I Morjan ◽  
T Dikonimos-Makris ◽  
...  
Keyword(s):  
Gas Phase ◽  
Ceramic Powder ◽  
Gas Phase Reactions ◽  
Powder Production

scholarly journals Cooperative Salt Bridge Stabilization of Gas-Phase Zwitterions in Neutral Arginine Clusters

2002 ◽  
Vol 106 (1) ◽  
pp. 32-34 ◽  
Author(s):  
Ryan R. Julian ◽  
J. L. Beauchamp ◽  
William A. Goddard
Keyword(s):  
Gas Phase ◽  
Salt Bridge

Methylene. III. Gas phase reactions with 1-chloropropane

1969 ◽  
Vol 312 (1509) ◽  
pp. 141-161 ◽  
Keyword(s):  
Gas Phase ◽  
Rate Constants ◽  
Hydrogen Abstraction ◽  
The Other ◽  
Gas Phase Reactions ◽  
Other Hand ◽  
Chlorine Substituent ◽  
High Degree ◽  
Singlet Methylene

The work described in this and the following paper is a continuation of that in parts I and II, devoted to elucidation of the mechanism of the reactions of methylene with chloroalkanes, with particular reference to the reactivities of singlet and triplet methylene in abstraction and insertion processes. The products of the reaction between methylene, prepared by the photolysis of ketene, and 1-chloropropane have been identified and estimated and their dependence on reactant pressures, photolysing wavelength and presence of foreign gases (oxygen and carbon mon­oxide) has been investigated. Both insertion and abstraction mechanisms contribute significantly to the over-all reaction, insertion being relatively much more important than with chloroethane. This type of process appears to be confined to singlet methylene. If, as seems likely, there is no insertion into C—Cl bonds under our conditions (see part IV), insertion into C2—H and C3—H bonds occurs in statistical ratio, approximately. On the other hand, the chlorine substituent reduces the probability of insertion into C—H bonds in its vicinity. As in the chloroethane system, both species of methylene show a high degree of selectivity in their abstraction reactions. We find that k S Cl / k S H >7.7, k T Cl / k T H < 0.14, where the k ’s are rate constants for abstraction, and the super- and subscripts indicate the species of methylene and the type of atom abstracted, respectively. Triplet methylene is discriminating in hydrogen abstraction from 1-C 3 H 7 Cl, the overall rates for atoms attached to C1, C2, C3 being in the ratios 2.63:1:0.

scholarly journals Gas-Phase Reactions between Urea and Ca2+:  The Importance of Coulomb Explosions

2004 ◽  
Vol 108 (46) ◽  
pp. 10080-10088 ◽  
Author(s):  
Inés Corral ◽  
Otilia Mó ◽  
Manuel Yáñez ◽  
Jean-Yves Salpin ◽  
Jeanine Tortajada ◽  
...  
Keyword(s):  
Gas Phase ◽  
Gas Phase Reactions
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