Electron attachment to strongly polar clusters Formamide molecule and clusters

نویسندگان

  • M. Seydou
  • A. Modelli
  • B. Lucas
  • K. Konate
  • C. Desfrançois
  • J. P. Schermann
چکیده

Electron localization is studied in formamide cluster anions. The isolated formamide molecule has a large dipole moment and its clusters can give birth to multipole-bound anions as well as valence anions. The vertical valence electron affinity of the isolated molecule is determined by electron transmission spectroscopy. The anion formation process is studied as a function of cluster size with Rydberg electron transfer spectroscopy. DFT calculations of the neutral and negatively-charged cluster structures show that the anion excess electron localizes on a single molecule. The adiabatic valence electron affinity of isolated formamide is deduced from the observation of the cluster size threshold for valence attachment. PACS. 34.80.Gs Molecular excitation and ionization by electron impact – 36.40.Mr Spectroscopy and geometrical structure of clusters – 87.15.By Structure and bonding

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Electron-triggered chemistry in HNO3/H2O complexes† †Electronic supplementary information (ESI) available: Mass spectrum from electron ionization of H2O/HNO3 complexes, benchmark calculations, and the calculated cluster structures. See DOI: 10.1039/c7cp01205e Click here for additional data file.

Polar stratospheric clouds, which consist mainly of nitric acid containing ice particles, play a pivotal role in stratospheric chemistry. We investigate mixed nitric acid-water clusters (HNO3)m(H2O)n, m ≈ 1-6, n ≈ 1-15, in a laboratory molecular beam experiment using electron attachment and mass spectrometry and interpret our experiments using DFT calculations. The reactions are triggered by th...

متن کامل

Investigation of structural and electronic properties of small Au n Cu m (n+m≤5) nano-clusters for Oxygen adsorption

In this study, the structures, the IR spectroscopy, and the electronic properties of AunCum (n+m≤5) bimetallic clusters were studied and compared with those of pure gold and copper clusters using the generalized gradient approximation (GGA) and exchange correlation density functional theory (DFT). The study of an O2-AunCum system is important to identify the promotion effects of each of the two...

متن کامل

Investigation of structural and electronic properties of small Au n Cu m (n+m≤5) nano-clusters for Oxygen adsorption

In this study, the structures, the IR spectroscopy, and the electronic properties of AunCum (n+m≤5) bimetallic clusters were studied and compared with those of pure gold and copper clusters using the generalized gradient approximation (GGA) and exchange correlation density functional theory (DFT). The study of an O2-AunCum system is important to identify the promotion effects of each of the two...

متن کامل

Excess electron localization sites in neutral water clusters.

We present approximate pseudopotential quantum-mechanical calculations of the excess electron states of equilibrated neutral water clusters sampled by classical molecular dynamics simulations. The internal energy of the clusters are representative of those present at temperatures of 200 and 300 K. Correlated electronic structure calculations are used to validate the pseudopotential for this pur...

متن کامل

Geometric and Electronic Structures of Vanadium Sub-nano Clusters, Vn (n = 2-5), and their Adsorption Complexes with CO and O2 Ligands: A DFT-NBO Study

In this study, electronic structures of ground state of pure vanadium sub-nano clusters, Vn (n=2-5), and their interactions with small ligands for example CO and triplet O2 molecules are investigated by using density functional theory (DFT) calibration at the mPWPW91/QZVP level of theory. The favorable orientations of these ligands in interaction with pure vanadium sub-nano clusters were determ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2005