TY - JOUR
T1 - Dissociation of dicarboxylate and disulfonate dianions
AU - Ard, S.
AU - Mirsaleh-Kohan, N.
AU - Steill, J.D.
AU - Oomens, J.
AU - Nielsen, S.B.
AU - Compton, R.N.
PY - 2010
Y1 - 2010
N2 - Collision-induced dissociation (CID), along with infrared multiple photon dissociation/detachment (IRMPD) techniques, is utilized to study a series of doubly substituted aromatic dianions containing sulfonate and carboxylate functionalities (1,2- and 1,3-benzenedisulfonate, 1,5-naphthalenedisulfonate, 2,6-naphthalenedisulfonate, 4-sulfobenzoate, 2,6-naphthalenedicarboxylate, and terephthalate dianions). The molecules were chosen because of the electronegativity of the CO
AB - Collision-induced dissociation (CID), along with infrared multiple photon dissociation/detachment (IRMPD) techniques, is utilized to study a series of doubly substituted aromatic dianions containing sulfonate and carboxylate functionalities (1,2- and 1,3-benzenedisulfonate, 1,5-naphthalenedisulfonate, 2,6-naphthalenedisulfonate, 4-sulfobenzoate, 2,6-naphthalenedicarboxylate, and terephthalate dianions). The molecules were chosen because of the electronegativity of the CO
U2 - 10.1063/1.3292577
DO - 10.1063/1.3292577
M3 - Article
SN - 0021-9606
VL - 132
SP - 094301
JO - Journal of Chemical Physics
JF - Journal of Chemical Physics
IS - 9
ER -
