Results 241 to 250 of about 54,172 (278)
Some of the next articles are maybe not open access.

Halogen bonding in solution

Chemical Society Reviews, 2012
Halogen bonding is the electron density donation based weak interaction of halogens with Lewis bases. Its applicability for molecular recognition processes long remained unappreciated and has so far mostly been studied in silico and in solid state.
Erdelyi, M.
openaire   +2 more sources

An overview of halogen bonding

Journal of Molecular Modeling, 2006
Halogen bonding (XB) is a type of noncovalent interaction between a halogen atom X in one molecule and a negative site in another. X can be chlorine, bromine or iodine.
Peter, Politzer   +4 more
openaire   +2 more sources

On The Nature of the Halogen Bond

Journal of Chemical Theory and Computation, 2014
The wide-ranging applications of the halogen bond (X-bond), notably in self-assembling materials and medicinal chemistry, have placed this weak intermolecular interaction in a center of great deal of attention. There is a need to elucidate the physical nature of the halogen bond for better understanding of its similarity and differences vis-à-vis other
Changwei, Wang   +3 more
openaire   +2 more sources

On the directionality of halogen bonding

Physical Chemistry Chemical Physics, 2013
The origin of the high directionality of halogen bonding was investigated quantum chemically by a detailed comparison of typical adducts in two different orientations: linear (most stable) and perpendicular. Energy decomposition analyses revealed that the synergy between charge-transfer interactions and Pauli repulsion are the driving forces for the ...
Stefan M, Huber   +4 more
openaire   +2 more sources

Halogen Bonding in Solution

2014
Because of its expected applicability for modulation of molecular recognition phenomena in chemistry and biology, halogen bonding has lately attracted rapidly increasing interest. As most of these processes proceed in solution, the understanding of the influence of solvents on the interaction is of utmost importance.
Anna-Carin C. Carlsson   +2 more
openaire   +2 more sources

Clˉ as the halogen bond acceptor: studies on strong halogen bonds

Structural Chemistry, 2017
The Clˉ anion as the halogen bond acceptor, the diiodotetrafluoroethane I(CF2)2I and its derivatives I(MF2)nI (M = C, Si, Ge, Sn) as the halogen bond donor, and the strong halogen bonds could be formed. The halogen bonds between I(MF2)nI and Clˉ have been designed and investigated by Moller–Plesset perturbation/aug-cc-pVDZ calculations together with ...
Jiaojiao Wang   +3 more
openaire   +1 more source

Biomolecular Halogen Bonds

2014
Halogens are atypical elements in biology, but are common as substituents in ligands, including thyroid hormones and inhibitors, which bind specifically to proteins and nucleic acids. The short-range, stabilizing interactions of halogens - now seen as relatively common in biology - conform generally to halogen bonds characterized in small molecule ...
openaire   +2 more sources

Halogen Bond Catalyzed Bromocarbocyclization

Angewandte Chemie International Edition, 2018
AbstractA halogen bond catalyzed bromo‐carbocyclization of N‐cinnamyl sulfonamides and O‐cinnamyl phenyl ethers has been developed. N‐methyl 4‐iodopyridinium triflate is used as the halogen‐bonding organocatalyst and the reaction is highly chemoselective.
Yuk‐Cheung Chan, Ying‐Yeung Yeung
openaire   +2 more sources

Halogen Bonding in a Crystalline Sponge

Inorganic Chemistry, 2019
Host-guest interactions are the key to the supramolecular chemistry and the further application of the receptors to study the structural details of the small guest molecules. Crystalline sponges as a kind of supramolecular receptor need to be investigated in terms of the binding ability with the guests.
Liangqian Yuan, Siyu Li, Fangfang Pan
openaire   +2 more sources

Halogen Bonding in Supramolecular Synthesis

2014
Supramolecular synthesis is typically limited to one-pot reactions because of the reversibility of non-covalent bonds, and to overcome this restriction we need to be able to rank the relative structural importance of such interactions and build synthetic methods to utilize synthons which can operate side-by-side without interference. Halogen bonds have
Christer B, Aakeröy   +1 more
openaire   +2 more sources

Home - About - Disclaimer - Privacy