Correlation between N 1s XPS Binding Energy and Bond Distance in Metal Amido, Imido, and Nitrido Complexes

2003 ◽  
Vol 42 (15) ◽  
pp. 4516-4518 ◽  
Author(s):  
Jin-Bao Wu ◽  
Yi-Feng Lin ◽  
Jelin Wang ◽  
Pei-Ju Chang ◽  
Chih-Pin Tasi ◽  
...  
Author(s):  
Tomas Baer ◽  
William L. Hase

Clusters are aggregates of loosely bonded molecules, in which each of the units retains the structure that it has as a free molecule. Because of the weak interactions among the molecules, clusters are stable only in cold environments such as are found in molecular beams. The weak intermolecular bonds provide an interesting testing ground for theories of intramolecular vibrational energy redistribution (IVR) and thus for theories of unimolecular dissociation. In addition, clusters constitute the bridge between the gas and liquid phases. Such phenomena as solvation, heat capacity, and phase transitions, which are ill defined for small clusters, become progressively more precise as the cluster size increases. Typical binding energies for neutral clusters are below 1000 cm-1. Ionic clusters, because of their ion-induced dipole forces, tend to be more strongly bonded with binding energies in excess of 5000 cm-1. Not infrequently, a neutral van der Waals dimer such as Ar2 with its binding energy of about 100 cm-1 (Tang and Toennies, 1986) changes its character upon ionization. The equilibrium bond distance is reduced from about 4 Å to 2.43 Å (Huber and Herzberg, 1979; Ma et al., 1993) and the binding energy increases to 10,000 cm-1 (Norwood et al., 1989; Furuya and Kimura, 1992). Clearly, the Ar2+ ion no longer meets our definition of a dimer. Rather, the neutral dimer is converted into a stable ion with a bond order of 1/2. A molecule that is frequently referred to as a cluster is C60. However, it is held together neither by weak bonds, nor is it composed of a collection of monomers. It is thus better classified as a large covalently bonded molecule. Table 10.1 summarizes some binding energies for various classes of dimers. When clusters comprise several loosely bound molecules, the atoms within each molecule are held together by strong bonds while the molecules themselves are attracted to neighboring molecules by weak bonds. This discrepancy in forces translates into disparities in the respective vibrational frequencies.


1992 ◽  
Vol 296 ◽  
Author(s):  
James J. Pinto

AbstractThe radiation stabilities of the nitramine explosives 1,4-dinitroglycolurile (DINGU), 1,4-dimethyl-2,5-dinitroglycolurile (DMD) and hexanitrohexaazaisowurtzitane (HNIW) have been determined using XPS. Samples were exposed to x-rays for times up to eight hours while photoelectron spectra were recorded in the carbon, oxygen, and nitrogen Is energy regions and mass spectra were recorded of gases evolved during the decomposition process. These data are compared to the previously determined stabilities for cyclotrimethylene trinitramine (RDX) and cyclotetramethylene tetranitramine (HlMX). The N1s spectra of the irradiated materials show the NO2 peak decreases relative to the total nitrogen signal while low binding energy peaks grow. The rate of loss of the NO2 peak was fit to first order kinetics and the rate constants obtained show some correlation with the N-N bond strength as measured by the average N-N bond distance and the average NO2 asymetric stretch frequency. Despite the differences in structure of these molecules (DINGU and DMD are bicyclic rings, RDX and HMX are rings and HNIW is a cage) the radiation stability appears to be controlled by the strength of the N-N bond.


1996 ◽  
Vol 166 (4) ◽  
pp. 447-448 ◽  
Author(s):  
Vladimir I. Belyavskii ◽  
Yurii V. Kopaev ◽  
N.V. Kornyakov

2016 ◽  
pp. 4024-4028 ◽  
Author(s):  
Sergey I. Pokutnyi ◽  
Wlodzimierz Salejda

The possibility of occurrence of the excitonic  quasimolecule formed of spatially separated electrons and holes in a nanosystem that consists  of  CuO quantum dots synthesized in a silicate glass matrix. It is shown that the major contribution to the excitonic quasimolecule binding energy is made by the energy of the exchange interaction of electrons with holes and this contribution is much more substantial than the contribution of the energy of Coulomb interaction between the electrons and holes.


Author(s):  
Akhileshwar Srivastava ◽  
Divya Singh

Presently, an emerging disease (COVID-19) has been spreading across the world due to coronavirus (SARS-CoV2). For treatment of SARS-CoV2 infection, currently hydroxychloroquine has been suggested by researchers, but it has not been found enough effective against this virus. The present study based on in silico approaches was designed to enhance the therapeutic activities of hydroxychloroquine by using curcumin as an adjunct drug against SARS-CoV2 receptor proteins: main-protease and S1 receptor binding domain (RBD). The webserver (ANCHOR) showed the higher protein stability for both receptors with disordered score (<0.5). The molecular docking analysis revealed that the binding energy (-24.58 kcal/mol) of hydroxychloroquine was higher than curcumin (-20.47 kcal/mol) for receptor main-protease, whereas binding energy of curcumin (<a>-38.84</a> kcal/mol) had greater than hydroxychloroquine<a> (-35.87</a> kcal/mol) in case of S1 receptor binding domain. Therefore, this study suggested that the curcumin could be used as combination therapy along with hydroxychloroquine for disrupting the stability of SARS-CoV2 receptor proteins


Author(s):  
A. S. Sharipov ◽  
◽  
B. I. Loukhovitski ◽  

The size-dependence of different physical properties of atomic clusters (by the example of binding energy, collision diameter, and static isotropic polarizability) is discussed.


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