Encapsulationof the Haloalkane 4‐Chloromethylpyridine Hydrochloride by Cucurbit[8]uril

[1]  Yu Liu,et al.  Photooxidation-Driven Purely Organic Room-Temperature Phosphorescent Lysosome-Targeted Imaging. , 2021, Journal of the American Chemical Society.

[2]  Zhiyong Zhao,et al.  Tunable White-Light Emissions of Azapyrene Derivatives with Cucurbit[n]uril Hosts in Aqueous Solution. , 2021, Organic letters.

[3]  Meilin Liu,et al.  Polymeric self-assembled cucurbit[n]urils: Synthesis, structures and applications , 2021 .

[4]  R. Chaâbane,et al.  In silico exploration of O-H…X2+ (X = Cu, Ag, Hg) interaction, targeted adsorption zone, charge density iso-surface, O-H proton analysis and topographic parameters theory for calix[6]arene and calix[8]arene as model , 2021, Journal of Molecular Liquids.

[5]  Meilin Liu,et al.  Recognition of glycine by cucurbit[5]uril and cucurbit[6]uril: A comparative study of exo- and endo-binding , 2021, Chinese Chemical Letters.

[6]  Yunqian Zhang,et al.  Pyridine Detection Using Supramolecular Organic Frameworks Incorporating Cucurbit[10]uril. , 2021, ACS applied materials & interfaces.

[7]  Z. Tao,et al.  Detecting Pesticide Dodine by Displacement of Fluorescent Acridine from Cucurbit[10]uril Macrocycle. , 2020, Journal of agricultural and food chemistry.

[8]  C. Przybylski,et al.  First Steps to Rationalize Host-Guest Interaction between α-, β-, and γ-Cyclodextrin and Divalent First-Row Transition and Post-transition Metals (Subgroups VIIB, VIIIB, and IIB). , 2020, Inorganic chemistry.

[9]  L. García‐Río,et al.  Cucurbit[7]uril as a Supramolecular Catalyst in Base-Catalyzed Reactions. Experimental and Theoretical Studies on Carbonate and Thiocarbonate Hydrolysis Reactions. , 2020, The Journal of organic chemistry.

[10]  Z. Tao,et al.  Selective recognition of tryptophan by a methylpillar[5]arene-based supramolecular fuorescent probe. , 2020, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.

[11]  Xi Zhang,et al.  Cucurbit[n]urils for supramolecular catalysis. , 2020, Chemistry.

[12]  Bei-bei Liu,et al.  A Biomimetic Model for the Active Site of [Fe]-H2ase Featuring a 2-Methoxy-3,5-dimethyl-4-phosphato-6-acylmethylpyridine Ligand , 2019, Organometallics.

[13]  V. Ramamurthy,et al.  Modulation of Reduction Potentials of Bis(pyridinium)alkane Dications through Encapsulation within Cucurbit[7]uril. , 2019, The Journal of organic chemistry.

[14]  Jing-lan Kan,et al.  Facile preparation and application of luminescent cucurbit[10]uril-based porous supramolecular frameworks , 2019, Sensors and Actuators B: Chemical.

[15]  Xiuping Chen,et al.  Supramolecular Encapsulation and Bioactivity Modulation of a Halonium Ion by Cucurbit[ n]uril ( n = 7, 8). , 2018, The Journal of organic chemistry.

[16]  I. Sterkhova,et al.  PCl3- and organometallic-free synthesis of tris(2-picolyl)phosphine oxide from elemental phosphorus and 2-(chloromethyl)pyridine hydrochloride , 2018 .

[17]  Kai Chen,et al.  Development of hydroxylated cucurbit[n]urils, their derivatives and potential applications , 2017 .

[18]  Zhong‐Zheng Gao,et al.  Host-guest complexation of cucurbit[8]uril with two enantiomers , 2017, Scientific Reports.

[19]  Shiguo Sun,et al.  Bromination of N-phenyloxypropyl-N′-ethyl-4,4′-bipyridium in cucurbit[8]uril molecular reactor , 2017 .

[20]  L. Lindoy,et al.  Twisted Cucurbit[n]urils. , 2016, Organic letters.

[21]  Yangjie Wu,et al.  Cucurbit[7]uril promoting PdCl2-catalyzed cross-coupling reaction of benzyl halides and arylboronic acids in aqueous media , 2014 .

[22]  Chris Toprakcioglu,et al.  Photocontrol over cucurbit[8]uril complexes: stoichiometry and supramolecular polymers. , 2013, Journal of the American Chemical Society.

[23]  Yunqian Zhang,et al.  Twisted cucurbit[14]uril. , 2013, Angewandte Chemie.

[24]  G. Wei,et al.  Encapsulation of adefovir bis(l-leucine propyl)ester pro-virucide in cucurbit[7]uril and its activity against tobacco mosaic virus , 2013 .

[25]  P. Zavalij,et al.  Cucurbit[10]uril. , 2005, Journal of the American Chemical Society.

[26]  P. Zavalij,et al.  The inverted cucurbit[n]uril family. , 2005, Journal of the American Chemical Society.

[27]  Barry B Snushall,et al.  Controlling factors in the synthesis of cucurbituril and its homologues. , 2001, The Journal of organic chemistry.

[28]  Eunsung Lee,et al.  New Cucurbituril Homologues: Syntheses, Isolation, Characterization, and X-ray Crystal Structures of Cucurbit[n]uril (n = 5, 7, and 8) , 2000 .