scholarly journals Conversion of non-covalent interactions in nucleoproteins into covalent bonds: Quantitative determination of protein covalently bound to polynucleotides

FEBS Letters ◽  
1974 ◽  
Vol 38 (3) ◽  
pp. 308-310 ◽  
Author(s):  
M.F. Turchinsky ◽  
E.I. Budowsky
Molecules ◽  
2021 ◽  
Vol 26 (5) ◽  
pp. 1305
Author(s):  
Stefano Borocci ◽  
Felice Grandinetti ◽  
Nico Sanna

The structure, stability, and bonding character of fifteen (Ng-H-Ng)+ and (Ng-H-Ng')+ (Ng, Ng' = He-Xe) compounds were explored by theoretical calculations performed at the coupled cluster level of theory. The nature of the stabilizing interactions was, in particular, assayed using a method recently proposed by the authors to classify the chemical bonds involving the noble-gas atoms. The bond distances and dissociation energies of the investigated ions fall in rather large intervals, and follow regular periodic trends, clearly referable to the difference between the proton affinity (PA) of the various Ng and Ng'. These variations are nicely correlated with the bonding situation of the (Ng-H-Ng)+ and (Ng-H-Ng')+. The Ng-H and Ng'-H contacts range, in fact, between strong covalent bonds to weak, non-covalent interactions, and their regular variability clearly illustrates the peculiar capability of the noble gases to undergo interactions covering the entire spectrum of the chemical bond.


2020 ◽  
Vol 22 (28) ◽  
pp. 16421-16430 ◽  
Author(s):  
Ibon Alkorta ◽  
J. Grant Hill ◽  
Anthony C. Legon

Alkali–metal bonds formed by LiR and NaR (R = F, H, CH3) with each of the Lewis bases OC, HCN, H2O, H3N, H2S and H3P are investigated ab initio at the CCSD(T)/AVTZ and CCSD(T)/awCVTZ levels to characterise these non-covalent interactions.


2010 ◽  
Vol 63 (4) ◽  
pp. 611 ◽  
Author(s):  
Jean-Marie Lehn

Dynamers are defined as constitutional dynamic polymers, i.e. polymeric entities whose monomeric components are linked through reversible connections and have therefore the capacity to modify their constitution by exchange and reshuffling of their components. They may be either of supramolecular or molecular nature depending on whether the connections are non-covalent interactions or reversible covalent bonds. They are formed respectively either by polyassociation with interactional recognition or by polycondensation with functional recognition between the connecting subunits. Both types are illustrated by specific examples implementing hydrogen bonding on one hand and formation of imine-type bonds on the other. The dynamic properties confer to dynamers the ability to undergo adaptation and driven evolution under the effect of external chemical or physical triggers. Dynamers thus are constitutional dynamic materials resulting from the application of the principles of constitutional dynamic chemistry to polymer science.


2016 ◽  
Vol 12 ◽  
pp. 1453-1458 ◽  
Author(s):  
Golo Storch ◽  
Sebastian Pallmann ◽  
Frank Rominger ◽  
Oliver Trapp

Stereodynamic ligands offer intriguing possibilities in enantioselective catalysis. “NU-BIPHEPs” are a class of stereodynamic diphosphine ligands which are easily accessible via rhodium-catalyzed double [2 + 2 + 2] cycloadditions. This study explores the preparation of differently functionalized “NU-BIPHEP(O)” compounds, the characterization of non-covalent adduct formation and the quantification of enantiomerization barriers. In order to explore the possibilities of functionalization, we studied modifications of the ligand backbone, e.g., with 3,5-dichlorobenzoyl chloride. Diastereomeric adducts with Okamoto-type cellulose derivatives and on-column deracemization were realized on the basis of non-covalent interactions. Enantioselective dynamic HPLC (DHPLC) allowed for the determination of rotational barriers of ΔG ‡ 298K = 92.2 ± 0.3 kJ mol−1 and 99.5 ± 0.1 kJ mol−1 underlining the stereodynamic properties of “NU-BIPHEPs” and “NU-BIPHEP(O)s”, respectively. These results make the preparation of tailor-made functionalized stereodynamic ligands possible and give an outline for possible applications in enantioselective catalysis.


Author(s):  
Abel M. Maharramov ◽  
Kamran T. Mahmudov ◽  
Maximilian N. Kopylovich ◽  
M. Fátima C. Guedes da Silva ◽  
Armando J. L. Pombeiro

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