Pure C-H hydrogen bonding to chloride ions: a preorganized and rigid macrocyclic receptor
about
Creating molecular macrocycles for anion recognitionSupramolecular chemistry: from aromatic foldamers to solution-phase supramolecular organic frameworksArtificial Molecular MachinesThe click reaction as an efficient tool for the construction of macrocyclic structuresMacrocycle Size Matters: “Small” Functionalized Rotaxanes in Excellent Yield Using the CuAAC Active Template ApproachReactions under the click chemistry philosophy employed in supramolecular and mechanostereochemical systems.Self-assembly and (hydro)gelation triggered by cooperative π-π and unconventional C-H···X hydrogen bonding interactions.Influence of the substitution and conformation of C--H-bond-based bis-triazole acceptors in anion-binding catalysis.Straightforward and Controlled Shape Access to Efficient Macrocyclic Imidazolylboronium Anion Receptors.Aryl C-H···Cl(-) hydrogen bonding in a fluorescent anion sensorMacrocyclic shape-persistency of cyclo[6]aramide results in enhanced multipoint recognition for the highly efficient template-directed synthesis of rotaxanes.Extremely strong tubular stacking of aromatic oligoamide macrocycles.A pyrrolyl-based triazolophane: a macrocyclic receptor with CH and NH donor groups that exhibits a preference for pyrophosphate anions10-(2-Pyrid-yloxy)phenanthren-9-ol.Living on the edge: Tuning supramolecular interactions to design two-dimensional organic crystals near the boundary of two stable structural phases.Benzene-, pyrrole-, and furan-containing diametrically strapped calix[4]pyrroles--an experimental and theoretical study of hydrogen-bonding effects in chloride anion recognition.Flexibility Coexists with Shape-Persistence in Cyanostar MacrocyclesNoncentrosymmetric Packings Influenced by Electronic Properties of Products of Click Reactions.Chemical sensors that incorporate click-derived triazoles.Shape persistence delivers lock-and-key chloride binding in triazolophanes.Click to bind: metal sensors.Beyond click chemistry - supramolecular interactions of 1,2,3-triazoles.Neutral CH and cationic CH donor groups as anion receptors.The btp [2,6-bis(1,2,3-triazol-4-yl)pyridine] binding motif: a new versatile terdentate ligand for supramolecular and coordination chemistry.Fluorescent Supramolecular Polymeric Materials.1,2,3,-Triazole-Based Catalysts: From Metal- to Supramolecular Organic Catalysis.New approaches to organocatalysis based on C-H and C-X bonding for electrophilic substrate activationSurveying macrocyclic chemistry: from flexible crown ethers to rigid cyclophanes.Multifunctional Tricarbazolo Triazolophane Macrocycles: One-Pot Preparation, Anion Binding, and Hierarchical Self-Organization of Multilayers.AuICl-bound N-heterocyclic carbene ligands form MII4(LAuCl)6 integrally gilded cages.1-(3-Bromo-prop-yl)-4-(2-pyrid-yl)-1H-1,2,3-triazole.Templated hierarchical self-assembly of poly(p-aryltriazole) foldamers.A ferrocene redox-active triazolium macrocycle that binds and senses chlorideSystematic replacement of amides by 1,4-disubstituted[1,2,3]triazoles in Leu-enkephalin and the impact on the delta opioid receptor activity.A cyclopeptide-derived molecular cage for sulfate ions that closes with a click.A bis(triazole)benzamide receptor for the complexation of halide anions and neutral carboxylic acid guests. Guest-controlled topicity and self-assembly.Tunable electronic interactions between anions and perylenediimide.Bidirectional regulation of halide binding in a heterometallic supramolecular cube.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.
P2860
Q26747283-FD1808AD-F65D-44BE-B906-D5BF8CC620B8Q26776192-B5E64B1A-7824-4332-92B4-CEA122A81729Q26783064-07DB96BD-3F9E-4E62-ADFC-2985D4B2C019Q26991854-C4A25F3C-ED4F-488B-A178-383A14B62DEBQ29040928-D842AF0E-8F5E-4C19-9CB2-C3A835B670F7Q30406660-046D46F8-565A-4C49-9381-7072AADAB9B6Q30718706-8441D6C5-4320-4DC2-8C1C-D5467D1DACBEQ30833949-FE99C8F2-B596-4638-88AE-CE8D74BEB90BQ31100654-E6B51C19-71C5-45BF-BD89-FB05E8A99277Q33576332-377400D2-A87A-4692-B548-802515EBD621Q33588383-ECACB8F0-7D03-49BC-9D00-38DAF56B51A6Q33655644-FB311155-FBB4-47ED-8FBE-0E2629BBF552Q34234911-9C356CB0-6E6A-4689-8C5A-97A4CF799384Q34431608-A3303758-41DF-4A0A-8B9E-D3D801206F77Q35082926-EAAAF8D4-E266-4126-9B5A-979D2D31C340Q36453088-21437185-1901-485E-BC04-922B2A793924Q37119658-5EF0F69B-2CC0-40CF-9A8F-B832943D0BB0Q37697078-B0ED80EA-4FA4-45CA-843D-16D863E73B2DQ37850327-5651D96F-E58F-4F58-8FF1-BCA14FB9C97FQ37976566-3C0A5DF6-810C-4555-8248-CFEF4FF9A62DQ38101542-39E740CF-14DD-4825-A7A6-9968B6DEF883Q38184880-A77E2D01-7C57-4F65-B46B-9B1847792EF6Q38215645-5DA5733A-25ED-4437-8475-708CBD68F82EQ38215659-EA9C08C0-65E2-45CD-ACF3-B201C8A06B97Q38757457-EFCCA5CE-D62F-421A-921A-5D436E9CA3E3Q38989386-93CB5B5C-C9D0-43AC-B57D-E4814E7B197CQ39112697-693C3C1F-E48E-4E7A-8D51-FC3E5F0D4087Q39277880-E6F2AFC8-662F-4BEA-9BA1-F4D1FAAF9C4EQ40290528-618F714A-595F-477E-B015-B739B439C92FQ41029036-13764C13-AD6D-4A16-B705-6EED7171C012Q41948369-156B3133-465F-485E-93CD-A265F6805425Q42269295-72FEFCC9-19BD-46F6-907A-B63CCD9D5FAAQ42584435-71B6115E-8B44-4D74-8501-82C63E0A1AA7Q42846104-B71C7246-2546-41B2-A22C-DD4C2169472AQ43063628-C59FDFDC-3767-473B-9EA3-EABA8C0E85FDQ43621261-C56435FB-CA9E-47FC-95A3-92B3F16A19DFQ43669541-191F3F07-DEC4-4F56-AA57-44320082C88CQ43760846-419E14B0-62A0-426E-90EA-5D9B1CA308B5Q43835921-73B648B2-ED1E-4B6D-B77B-7781C29198B7Q44125875-94363CA5-F4BB-4A9F-BEDA-D90E69376D71
P2860
Pure C-H hydrogen bonding to chloride ions: a preorganized and rigid macrocyclic receptor
description
wetenschappelijk artikel
@nl
наукова стаття, опублікована у 2008
@uk
name
Pure C-H hydrogen bonding to chloride ions: a preorganized and rigid macrocyclic receptor
@en
Pure C-H hydrogen bonding to chloride ions: a preorganized and rigid macrocyclic receptor
@nl
type
label
Pure C-H hydrogen bonding to chloride ions: a preorganized and rigid macrocyclic receptor
@en
Pure C-H hydrogen bonding to chloride ions: a preorganized and rigid macrocyclic receptor
@nl
prefLabel
Pure C-H hydrogen bonding to chloride ions: a preorganized and rigid macrocyclic receptor
@en
Pure C-H hydrogen bonding to chloride ions: a preorganized and rigid macrocyclic receptor
@nl
P356
P1476
Pure C-H hydrogen bonding to chloride ions: a preorganized and rigid macrocyclic receptor
@en
P2093
Amar H Flood
Yongjun Li
P2860
P304
P356
10.1002/ANIE.200704717
P407
P577
2008-01-01T00:00:00Z