An intramolecular hydrogen bond study in some Schiff bases of fulvene: a challenge between the RAHB concept and the σ-skeleton influence

2014 ◽  
Vol 38 (12) ◽  
pp. 5886-5891 ◽  
Author(s):  
A-Reza Nekoei ◽  
Morteza Vatanparast

DFT, NBO and AIM analyses have been employed to investigate which one, the resonance-assisted hydrogen bond concept or the σ-skeleton of the system, has more influence on making intramolecular hydrogen bonds stronger.

2019 ◽  
Vol 43 (33) ◽  
pp. 13134-13142 ◽  
Author(s):  
Neeru Arya ◽  
Sandeep Kumar Mishra ◽  
N. Suryaprakash

The extensive NMR investigations reveal the presence of E-isomers in the derivative of N′-benzylidenebenzohydrazide. The different conformer populations are controlled by the strength of intramolecular hydrogen bonds.


2013 ◽  
Vol 68 (3) ◽  
pp. 214-222 ◽  
Author(s):  
Jörg Hübscher ◽  
Michael Günthel ◽  
Robert Rosin ◽  
Wilhelm Seichter ◽  
Florian Mertens ◽  
...  

Two new linker-type molecules 1a and 1b composed of o-hydroxyacetophenone coordinative groups attached to linear ethynylene or 1,4-phenylenediethynylene spacer units have been synthesised and structurally characterised. An X-ray crystallographic study for both compounds has shown structures with strong intramolecular hydrogen bonds fitting in the model of ‘Intramolecular Resonance Assisted Hydrogen Bond (IRHAB)’. Initial coordination experiments with Cu(II) were performed and the resulting materials characterised by PXRD. The similarity of the copper coordination between these compounds and copper(II) acetylacetonate complexes was demonstrated by XPS measurements. Based on the evidence of these studies, and on elemental analysis, the formation of the corresponding coordination polymers comprising Cu(II) and the linkers has been proposed


2018 ◽  
Vol 212 ◽  
pp. 399-419 ◽  
Author(s):  
Feriel BenNasr ◽  
Ariel Pérez-Mellor ◽  
Ivan Alata ◽  
Valeria Lepere ◽  
Nejm-Eddine Jaïdane ◽  
...  

Changing the chirality of one residue prevents the formation of an OH⋯O intramolecular hydrogen bond in cyclo di-tyrosine.


2022 ◽  
Author(s):  
Asia Marie S Riel ◽  
Daniel Adam Decato ◽  
Jiyu Sun ◽  
Orion Berryman

Recent results indicate a halogen bond donor is strengthened through direct interaction with a hydrogen bond to the electron-rich belt of the halogen. Here, this Hydrogen Bond enhanced Halogen Bond...


2020 ◽  
Vol 7 (19) ◽  
pp. 3548-3554
Author(s):  
Keke Wang ◽  
Qunmin Wang ◽  
Xiong Wang ◽  
Mei Wang ◽  
Qin Wang ◽  
...  

Intramolecular hydrogen bonds in ligands restrict the rotation of carboxyl groups and consequently enhance the chemical stability of MOFs.


Author(s):  
Galal H. Elgemeie ◽  
Shahinaz H. Sayed ◽  
Peter G. Jones

The title compound, C10H11N3O3S, (I), crystallizes as the NH tautomer. The two rings subtend an interplanar angle of 72.54 (4)°. An intramolecular hydrogen bond is formed from the NH2group to a sulfonyl O atom. The molecular packing involves layers of molecules parallel to thebcplane atx≃ 0, 1etc., with two classical linear hydrogen bonds (amino–sulfonyl and pyrazoline–carbonyl N—H...O) and a further interaction (amino–sulfonyl N—H...O) completing a three-centre system with the intramolecular contact. The analogous phenyl derivative, (II) [Elgemeie, Hanfy, Hopf & Jones (1998).Acta Cryst.C54, 136–138], crystallizes with essentially the same unit cell and packing pattern, but with two independent molecules that differ significantly in the orientation of the phenyl groups. The space group isP21/cfor (I) butP21for (II), which is thus a pseudosymmetric counterpart of (I).


1998 ◽  
Vol 444 (1-3) ◽  
pp. 221-225 ◽  
Author(s):  
Zbigniew Rozwadowski ◽  
Teresa Dziembowska ◽  
Grzegorz Schroeder ◽  
Bogumil Brzezinski

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