Ab initio theoretical study of dipole-bound anions of molecular complexes. Water molecule inhibits or enhances electron affinity of N-methylaminoadenine

J. Smets, D. M A Smith, Y. Elkadi, Ludwik Adamowicz

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Ab initio calculations have been performed to determine the electron affinity of the water complex of N-methylaminoadenine (NMA). This complex has been chosen for this study because it can form three different isomeric structures with a water molecule hydrogen-bonded at three different NMA sites, and only two of these structures have sufficient dipole moments to form dipole-bound states with an excess electron. In the third structure, which according to the calculations should be the most stable form, the dipole moments of NMA and the water molecule oppose each other resulting in an almost null dipole moment of the complex, so the complex has no ability to form a stable dipole-bound anion. This determination offers an interesting possibility for an experimental investigation of whether the NMA.H2O complex forms an stable anion. If such an anion is detected, it will mean that an electron attachment can increase the gas- phase concentration of the complex, which is thermodynamically less stable in its neutral form.

Original languageEnglish (US)
Pages (from-to)1615-1623
Number of pages9
JournalPolish Journal of Chemistry
Volume72
Issue number7 SUPPL.
StatePublished - Jul 1998

Fingerprint

Electron affinity
Dipole moment
Anions
Molecules
Water
Electrons
Hydrogen
Gases

Keywords

  • Dipole moment
  • Dipole-bound state
  • Electron affinity
  • Hydrogen bond
  • Molecular anion

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Ab initio theoretical study of dipole-bound anions of molecular complexes. Water molecule inhibits or enhances electron affinity of N-methylaminoadenine. / Smets, J.; Smith, D. M A; Elkadi, Y.; Adamowicz, Ludwik.

In: Polish Journal of Chemistry, Vol. 72, No. 7 SUPPL., 07.1998, p. 1615-1623.

Research output: Contribution to journalArticle

@article{3dcaedabf9fb4892ab0a7b3edb4e0dab,
title = "Ab initio theoretical study of dipole-bound anions of molecular complexes. Water molecule inhibits or enhances electron affinity of N-methylaminoadenine",
abstract = "Ab initio calculations have been performed to determine the electron affinity of the water complex of N-methylaminoadenine (NMA). This complex has been chosen for this study because it can form three different isomeric structures with a water molecule hydrogen-bonded at three different NMA sites, and only two of these structures have sufficient dipole moments to form dipole-bound states with an excess electron. In the third structure, which according to the calculations should be the most stable form, the dipole moments of NMA and the water molecule oppose each other resulting in an almost null dipole moment of the complex, so the complex has no ability to form a stable dipole-bound anion. This determination offers an interesting possibility for an experimental investigation of whether the NMA.H2O complex forms an stable anion. If such an anion is detected, it will mean that an electron attachment can increase the gas- phase concentration of the complex, which is thermodynamically less stable in its neutral form.",
keywords = "Dipole moment, Dipole-bound state, Electron affinity, Hydrogen bond, Molecular anion",
author = "J. Smets and Smith, {D. M A} and Y. Elkadi and Ludwik Adamowicz",
year = "1998",
month = "7",
language = "English (US)",
volume = "72",
pages = "1615--1623",
journal = "Polish Journal of Chemistry",
issn = "0137-5083",
publisher = "Polish Chemical Society",
number = "7 SUPPL.",

}

TY - JOUR

T1 - Ab initio theoretical study of dipole-bound anions of molecular complexes. Water molecule inhibits or enhances electron affinity of N-methylaminoadenine

AU - Smets, J.

AU - Smith, D. M A

AU - Elkadi, Y.

AU - Adamowicz, Ludwik

PY - 1998/7

Y1 - 1998/7

N2 - Ab initio calculations have been performed to determine the electron affinity of the water complex of N-methylaminoadenine (NMA). This complex has been chosen for this study because it can form three different isomeric structures with a water molecule hydrogen-bonded at three different NMA sites, and only two of these structures have sufficient dipole moments to form dipole-bound states with an excess electron. In the third structure, which according to the calculations should be the most stable form, the dipole moments of NMA and the water molecule oppose each other resulting in an almost null dipole moment of the complex, so the complex has no ability to form a stable dipole-bound anion. This determination offers an interesting possibility for an experimental investigation of whether the NMA.H2O complex forms an stable anion. If such an anion is detected, it will mean that an electron attachment can increase the gas- phase concentration of the complex, which is thermodynamically less stable in its neutral form.

AB - Ab initio calculations have been performed to determine the electron affinity of the water complex of N-methylaminoadenine (NMA). This complex has been chosen for this study because it can form three different isomeric structures with a water molecule hydrogen-bonded at three different NMA sites, and only two of these structures have sufficient dipole moments to form dipole-bound states with an excess electron. In the third structure, which according to the calculations should be the most stable form, the dipole moments of NMA and the water molecule oppose each other resulting in an almost null dipole moment of the complex, so the complex has no ability to form a stable dipole-bound anion. This determination offers an interesting possibility for an experimental investigation of whether the NMA.H2O complex forms an stable anion. If such an anion is detected, it will mean that an electron attachment can increase the gas- phase concentration of the complex, which is thermodynamically less stable in its neutral form.

KW - Dipole moment

KW - Dipole-bound state

KW - Electron affinity

KW - Hydrogen bond

KW - Molecular anion

UR - http://www.scopus.com/inward/record.url?scp=0032353548&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0032353548&partnerID=8YFLogxK

M3 - Article

VL - 72

SP - 1615

EP - 1623

JO - Polish Journal of Chemistry

JF - Polish Journal of Chemistry

SN - 0137-5083

IS - 7 SUPPL.

ER -