PNNL

Abstract

This work reports a systematic photoelectron spectroscopy and theoretical investigation on the electronic and geometric structures of four doubly deprotonated 2’-deoxynucleoside 5’-monophosphate dianions, the smallest quintessential DNA building block. These dianions are intrinsically stable with their adiabatic/vertical detachment energies (ADE/VDE) ranging from 0.85/1.07 (A), 1.05/1.30 (G) to 1.20/1.50 (C) and 1.80/2.10 eV (T). The repulsive Coulomb barrier against electron detachment is 2.0 eV for purines and 2.5 eV for pyrimidines. Dianions are deprotonated at the phosphate group and the amino group of a nucleobase. The calculated ADE/VDE values, as well as the simulated spectrum, agree well with the experimental results. The ?-type HOMO orbital resides on the nucleobase moiety for each dianion. This spatial distribution of HOMO suggests that the most loosely bound electron is detached along the direction perpendicular to the nucleobase. When combined with the previous results this work makes complete the depiction of basic building blocks of DNA at the molecular level.