The fragmentation of melamine: A study via electron-impact ionization, laser-desorption ionization, collision-induced dissociation, and density functional calculations of potential energy surface
Ss. Ju et al., The fragmentation of melamine: A study via electron-impact ionization, laser-desorption ionization, collision-induced dissociation, and density functional calculations of potential energy surface, J PHYS CH B, 103(3), 1999, pp. 582-596
We have studied the fragmentation of the melamine (2,4,6-triamino-s-triazin
e) molecule and its deuterated counterparts via electron impact ionization
(ET), laser desorption ionization (LDI), and collision-induced dissociation
(CID). Our EI and LDI measurements show that the dissociation of melamine
is different from the concerted triple dissociation pathway of s-triazine.
In EI experiments, the protonated and parent melamine ion (m/z = 127 (C3N6H
7+) and 126 (C3N6H6+)) were formed initially with 20 and 70 eV electron bom
bardment. Other fragment ions, such as m/z = 43 (CN2H3+), 53 (C2N2H+), 56 (
CN3H2+), 68 (C2N3H2+), 83 (C2N4H3+), 85 (C2N4H5+), 99 (C2N5H5+), 110 (C3N5H
4+), etc., were subsequently formed from the decomposition of metastable me
lamine ions. This speculation was supported by our additional CID measureme
nts. On the other hand, in the LDI experiments the melamine molecule was pu
mped to 1(1)A " and 2(1)A' excited electronic states, respectively, with 26
6 and 193 nm lasers. In view of the same fragment ions (m/z = 43, 45 (CN2H5
+), 60 (CN3H6+), 85, and 127) resulting from the different excited 1(1)A "
and 2(1)A' states, we conclude that the fragmentation of melamine in LDI pr
oceeds via internal conversion to its ground potential energy surface (1(1)
A') prior to dissociation. The decomposition mechanism in the ground electr
onic state has been investigated using the density functional B3LYP/6-31G*
and B3LYP/cc-pVTZ methods. All the molecular ions observed in EI experiment
s can be produced from major and minor neutral fragments of melamine dissoc
iation. The calculations demonstrate the reaction pathways leading to these
fragments and predict the corresponding activation energies. The dissociat
ion mechanism of melamine is shown to be distinct from that of s-triazine,
because of the presence of mobile hydrogen atoms in the amino groups.