scholarly journals Recognition of a cognate RNA aptamer by neomycin B: quantitative evaluation of hydrogen bonding and electrostatic interactions

2000 ◽  
Vol 28 (15) ◽  
pp. 2935-2942 ◽  
Author(s):  
J. A. Cowan
2001 ◽  
Vol 13 (5) ◽  
pp. 619-625 ◽  
Author(s):  
Alex Fragoso ◽  
Roberto Cao ◽  
Alicia Díz ◽  
Ileana Sånchez ◽  
Leticia Sånchez

2016 ◽  
Vol 408 (13) ◽  
pp. 3593-3600 ◽  
Author(s):  
Kai Ling ◽  
Hongyan Jiang ◽  
Linlin Zhang ◽  
Yang Li ◽  
Lu Yang ◽  
...  

CrystEngComm ◽  
2015 ◽  
Vol 17 (20) ◽  
pp. 3768-3771 ◽  
Author(s):  
Antonio Bauzá ◽  
Antonio Frontera ◽  
Tiddo J. Mooibroek ◽  
Jan Reedijk

A CSD analysis and DFT study reveal that the nitrogen lone-pair in [N(PPh3)2]+ is partially intact and involved in intramolecular hydrogen bonding.


Author(s):  
Bruce C. Bunker ◽  
William H. Casey

Water is one of the most complex fluids on Earth. Even after intense study, there are many aspects regarding the structure, properties, and chemistry of water that are not well understood. In this chapter, we highlight the attributes of water that dictate many of the reactions that take place between water and oxides. We start with a single water molecule and progress to water clusters, then finally to extended liquid and solid phases. This chapter provides a baseline for evaluating what happens when water encounters simple ions, soluble oxide complexes called hydrolysis products, and extended oxide phases. The primary phenomenon highlighted in this chapter is hydrogen bonding. Hydrogen bonding dominates the structure and properties of water and influences many water–oxide interactions. A single water molecule has eight valence electrons around a central oxygen anion. These electrons are contained in four sp3-hybridized molecular orbitals arranged as lobes that extend from the oxygen in a tetrahedral geometry. Each orbital is occupied by two electrons. Two of the lobes are bonded to protons; the other two lobes are referred to as lone pairs of electrons. The H–O–H bond angle of 104.5° is close to the tetrahedral angle of 109.5°. The O–H bond length in a single water molecule is 0.96 Ǻ. It is important to recognize that this bond length is really a measure of the electron density associated with the oxygen lone pair bonded to the proton. This is because a proton is so incredibly small (with an ionic radius of only 1.3·10−5 Ǻ) that it makes no contribution to the net bond length. The entire water molecule has a hard sphere diameter of 2.9 Ǻ, which is fairly typical for an oxygen anion. This means the unoccupied lone pairs are distended relative to the protonated lone pairs, extending out to roughly 1.9 Ǻ. The unequal distribution of charges introduces a dipole within the water molecule that facilitates electrostatic interactions with other molecules.


2009 ◽  
Vol 9 (12) ◽  
pp. 5009-5013 ◽  
Author(s):  
Marcos D. García ◽  
Víctor Blanco ◽  
Carlos Platas-Iglesias ◽  
Carlos Peinador ◽  
José M. Quintela

2018 ◽  
Vol 54 (64) ◽  
pp. 8845-8848 ◽  
Author(s):  
Miao Yu ◽  
Youness Benjalal ◽  
Chong Chen ◽  
Nataliya Kalashnyk ◽  
Wei Xu ◽  
...  

Ni adatoms are at the origin of a self-assembled bicomponent molecular system on Au(111).


2005 ◽  
Vol 58 (6) ◽  
pp. 442 ◽  
Author(s):  
John F. Quinn ◽  
Frank Caruso

Multilayer thin films were prepared based on hydrogen bonding between poly(N-isopropylacrylamide) (PNiPAAm), and poly(styrene sulfonate-co-maleic acid) (PSSMA). Since PSSMA is capable of associating with other polymers through both hydrogen bonding and electrostatic interactions, multilayer assemblies incorporating PSSMA, PNiPAAm, and intercalated poly(allylamine hydrochloride) (PAH) layers were also prepared. Intercalated PAH layers were included to improve the pH stability of the film by introducing electrostatic linkages into the assembly. Film construction was studied as a function of pH of the deposition solution and the number of inserted PAH layers. Film morphology varied significantly with incorporation of PAH into the film. It was also demonstrated that by intercalating several PAH layers within the PNiPAAm/PSSMA assembly, the pH stability of the films at pH 5.8 could be substantially improved.


1990 ◽  
Vol 55 (7) ◽  
pp. 2227-2229 ◽  
Author(s):  
Michael H. Abraham ◽  
Priscilla L. Grellier ◽  
David V. Prior ◽  
Jeffrey J. Morris ◽  
Peter J. Taylor ◽  
...  

IUCrData ◽  
2018 ◽  
Vol 3 (1) ◽  
Author(s):  
Alan M. Boltin ◽  
Gary L. Guillet

The title complex, [Li2Ni(C11H21N3Si2)2(C4H8O)2], is a trimetallic complex of two LiIcations and a NiIIcation bridged by twoN,N′-(pyridine-2,6-diyl)bis(trimethylsilylamide) ligands that crystallizes in theFdd2 space group. The molecule hasC2rotational symmetry, with the NiIIcation located on the twofold axis. The coordination sphere of the NiIIcation is composed of two amido N and two pyridyl N-atom donors in a distorted square-planar geometry. The LiIcations are coordinated by two amido N-atom donors and a tetrahydrofuran molecule with a long interaction with a pyridyl N-atom donor. The coordinating tetrahydrofuran ligand and a trimethylsilyl group are disordered. Intra- or intermolecular hydrogen bonding, as well as π–π stacking, are not observed between the molecules, likely indicating that weak electrostatic interactions are the dominant feature leading to the crystal structure.


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