A catenane assembled through a single charge-assisted halogen bond.
about
Evidence for halogen bond covalency in acyclic and interlocked halogen-bonding receptor anion recognitionSelective Nitrate Recognition by a Halogen-Bonding Four-Station [3]Rotaxane Molecular Shuttle.Progress in the synthesis and exploitation of catenanes since the Millennium.Molecular recognition in chemical and biological systems.Catenanes: fifty years of molecular links.The atom, the molecule, and the covalent organic framework.Halogen bonding molecular capsules.pH controlled assembly of a self-complementary halogen-bonded dimer.Neutral iodotriazoles as scaffolds for stable halogen-bonded assemblies in solution.Chloride-Anion-Templated Synthesis of a Strapped-Porphyrin-Containing Catenane Host System.Halogen- and hydrogen-bonding catenanes for halide-anion recognition.C-I...NC halogen bonding in two polymorphs of the mixed-valence 2:1 charge-transfer salt (EDT-TTF-I2)2(TCNQF4), with segregated versus alternated stacks.Ion-Pair Halogen Bonds in 2-Halo-Functionalized Imidazolium Chloride Receptors: Substituent and Solvent Effects.Halogen-Bonded Supramolecular Capsules in the Solid State, in Solution, and in the Gas Phase.Chiral Catenanes and Rotaxanes: Fundamentals and Emerging Applications.Formation of Self-Templated 2,6-Bis(1,2,3-triazol-4-yl)pyridine [2]Catenanes by Triazolyl Hydrogen Bonding: Selective Anion Hosts for Phosphate.A Fluorescent Ditopic Rotaxane Ion Pair Host.Competition between hydrogen bonds and halogen bonds in complexes of formamidine and hypohalous acids.Catalytic enantioselective alkylation of sulfenate anions to chiral heterocyclic sulfoxides using halogenated pentanidium salts.Halogen bonded supramolecular capsules: a challenging test case for quantum chemical methods.Charge-assisted halogen bonding: donor-acceptor complexes with variable ionicity.A smart "off-on" gate for the in situ detection of hydrogen sulphide with Cu(ii)-assisted europium emission.
P2860
Q35005970-C3014E28-235B-406D-A1C1-A9D1A48311C2Q37420560-B175A107-D57A-4C00-B32E-30857BCCBAAEQ38199961-F1A62C6F-BEB5-49E9-9ED8-6AFE8C66CF32Q38335784-2DF4DA8F-F85C-4C88-8DCA-874F2DC19695Q38464452-A6D41EE6-1FFB-496C-88C5-F4A2FC46DE72Q39158837-06DF1462-F735-41B6-9035-2D9DA9913A9FQ40899852-07480B16-5B12-4087-BDF4-8A4374907A20Q42233270-B2E66601-1844-45EF-A557-2727F423ECEEQ42315611-29DEDBFC-2B65-4147-81C4-834BCAD47AE6Q42663834-AEA4A053-E191-438B-AF31-55ED3A0F6522Q46885524-6F5D2DD2-7D60-498F-A50F-012C14B05E64Q46944449-BCF23F2B-5511-4744-9B74-928DF95BFCEAQ48095912-B19E0A1A-AB5F-4390-8619-5EC867C463AFQ48130685-8C51108B-B0EA-4484-A703-8ADF9C4FB7F1Q48155264-5AEE65AF-5F80-4AD6-9B30-74C1C8406284Q48202290-4C033CD3-5436-433E-A825-282A7D5A327DQ49375307-0394F4FB-F139-4AF0-8520-3EB4B8F1401CQ50230209-9C97CB4C-1AF5-4E3F-8D7C-601FC684FD07Q51039945-27C901F3-35DD-44DF-A346-1D96190263A0Q54239622-BD0C0361-A90A-490F-8402-38449AC4D36AQ54293052-DDE0AD61-2432-4CE0-8078-87279170159CQ55280369-D9DF7244-2C7C-4310-9527-D371B778C5E5
P2860
A catenane assembled through a single charge-assisted halogen bond.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
A catenane assembled through a single charge-assisted halogen bond.
@en
type
label
A catenane assembled through a single charge-assisted halogen bond.
@en
prefLabel
A catenane assembled through a single charge-assisted halogen bond.
@en
P2093
P2860
P50
P356
P1476
A catenane assembled through a single charge-assisted halogen bond
@en
P2093
Lydia C Gilday
Paul D Beer
Thomas Lang
P2860
P304
P356
10.1002/ANIE.201300464
P407
P577
2013-03-11T00:00:00Z