Aromatic and aliphatic CH hydrogen bonds fight for chloride while competing alongside ion pairing within triazolophanes - Wikidata - awgldk - TriplyDB

Aromatic and aliphatic CH hydrogen bonds fight for chloride while competing alongside ion pairing within triazolophanes

Aromatic and aliphatic CH hydrogen bonds fight for chloride while competing alongside ion pairing within triazolophanes

http://www.wikidata.org/entity/Q57110442

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Creating molecular macrocycles for anion recognition Interaction between anions and cationic metal complexes containing tridentate ligands with exo-C-H groups: complex stability and hydrogen bonding.Anion-induced dimerization of 5-fold symmetric cyanostars in 3D crystalline solids and 2D self-assembled crystals.Evidence for halogen bond covalency in acyclic and interlocked halogen-bonding receptor anion recognition Ion Pairing and Co-facial Stacking Drive High-Fidelity Bisulfate Assembly with Cyanostar Macrocyclic Hosts.Flexibility Coexists with Shape-Persistence in Cyanostar Macrocycles Shape persistence delivers lock-and-key chloride binding in triazolophanes.Anion receptor chemistry: highlights from 2011 and 2012.Beyond click chemistry - supramolecular interactions of 1,2,3-triazoles.Multifunctional Tricarbazolo Triazolophane Macrocycles: One-Pot Preparation, Anion Binding, and Hierarchical Self-Organization of Multilayers.A palladium nanoparticle-nanomicelle combination for the stereoselective semihydrogenation of alkynes in water at room temperature Substituent Effects in CH Hydrogen Bond Interactions: Linear Free Energy Relationships and Influence of Anions Increased halide recognition strength by enhanced intercomponent preorganisation in triazolium containing [2]rotaxanes.From atomic to molecular anions: a neutral receptor captures cyanide using strong C-H hydrogen bonds.Lasagna-type arrays with halide-nitromethane cluster filling. The first recognition of the Hal(-)···HCH2NO2 (Hal = Cl, Br, I) hydrogen bonding.Anions Stabilize Each Other inside Macrocyclic Hosts.An aryl-triazole foldamer containing a 1,8-naphthalimide fluorescent motif for monitoring and enhancing the anion-induced folding.[1₄]Heterophane prototypes containing azolium and/or azole anion-binding motifs.A rotaxane host system containing integrated triazole C-H hydrogen bond donors for anion recognition.Anion binding in aqueous media by a tetra-triazolium macrocycle.Anion effects on the cyclobis(paraquat-p-phenylene) host Two levels of conformational pre-organization consolidate strong CH hydrogen bonds in chloride-triazolophane complexes

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P2860

Aromatic and aliphatic CH hydrogen bonds fight for chloride while competing alongside ion pairing within triazolophanes

http://www.wikidata.org/entity/Q57110442

description

im Januar 2011 veröffentlichter wissenschaftlicher Artikel

@de

wetenschappelijk artikel

@nl

наукова стаття, опублікована в січні 2011

@uk

name

Aromatic and aliphatic CH hydr ...... pairing within triazolophanes

@en

Aromatic and aliphatic CH hydr ...... pairing within triazolophanes

@nl

type

label

Aromatic and aliphatic CH hydr ...... pairing within triazolophanes

@en

Aromatic and aliphatic CH hydr ...... pairing within triazolophanes

@nl

prefLabel

Aromatic and aliphatic CH hydr ...... pairing within triazolophanes

@en

Aromatic and aliphatic CH hydr ...... pairing within triazolophanes

@nl

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Chemistry: A European Journal

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Aromatic and aliphatic CH hydr ...... pairing within triazolophanes

@en

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Amar H Flood

http://www.w3.org/2001/XMLSchema#string

Esther O Uduehi

http://www.w3.org/2001/XMLSchema#string

Jonathan A Karty

http://www.w3.org/2001/XMLSchema#string

Krishnan Raghavachari

http://www.w3.org/2001/XMLSchema#string

Raghunath O Ramabhadran

http://www.w3.org/2001/XMLSchema#string

Yuran Hua

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P2860

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Squaraine rotaxane as a reversible optical chloride sensor.

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312-21

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scholarly article

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10.1002/CHEM.201002340

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1

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17

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2011-01-03T00:00:00Z

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21207627

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