Calixarene-Based Nanoscale Coordination Cages

被引：209

作者：

Liu, Mei ^{[1
,3
]}

Liao, Wuping ^{[1
]}

Hu, Chunhua ^{[2
]}

Du, Shangchao ^{[1
,3
]}

Zhang, Hongjie ^{[1
]}

机构：

[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Peoples R China

[2] NYU, Dept Chem, New York, NY 10003 USA

[3] Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China

来源：

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION | 2012年 / 51卷 / 07期

基金：

中国国家自然科学基金;

关键词：

cage compounds; calixarenes; cobalt; crystal engineering; tripodal ligands; METAL-ORGANIC FRAMEWORKS; RETICULAR SYNTHESIS; SORPTION PROPERTIES; TRANSITION-METAL; MOLECULAR CAGE; POLYHEDRA; LIGAND; CHEMISTRY; CAPSULES; CAVITAND;

D O I：

10.1002/anie.201106732

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Molecular shuttlecocks: The introduction of tripodal ternary acids (red; see picture) to the cobalt/calixarene (green) systems led to the formation of four unprecedented calixarene-based nanoscale coordination cages through a [6+8] condensation. The overall periphery diameters of the nanocages ranged from 3.3 to 4.7 nm, and there were two sizes for the internal cavities (1.1 and 1.7 nm). Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

引用

页码：1585 / 1588

页数：4

共 50 条

[31] Surface grafting and reactivity of calixarene-based receptors and pseudorotaxanes on Si(100)
Boccia, Alice
Lanzilotto, Valeria
Zanoni, Robertino
Pescatori, Luca
Arduini, Arturo
Secchi, Andrea
[J]. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2011, 13 (10) : 4444 - 4451
[32] Coordination Polymers based on calixarene derivatives: Structures and properties
Ovsyannikov, Alexander
Solovieva, Svetlana
Antipin, Igor
Ferlay, Sylvie
[J]. COORDINATION CHEMISTRY REVIEWS, 2017, 352 : 151 - 186
[33] FLOW-INJECTION ANALYSIS WITH TETRAMERIC CALIXARENE-BASED POTENTIOMETRIC DETECTION
TELTINGDIAZ, M
DIAMOND, D
SMYTH, MR
[J]. ANALYTICA CHIMICA ACTA, 1991, 251 (1-2) : 149 - 155
[34] Calixarene-based copper(I) complexes as models for monocopper sites in enzymes
Blanchard, S
Le Clainche, L
Rager, MN
Chansou, B
Tuchagues, JP
Duprat, AF
Le Mest, Y
Reinaud, O
[J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1998, 37 (19) : 2732 - 2735
[35] Calixarene-based picolinamide extractants for selective An/Ln separation from radioactive waste
Casnati, A
Della Ca', N
Fontanella, M
Sansone, F
Ugozzoli, F
Ungaro, R
Liger, K
Dozol, JF
[J]. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2005, 2005 (11) : 2338 - 2348
[36] Calixarene-based extractants for heavy metal ions removal from aqueous solutions
Konczyk, Joanna
Nowik-Zajac, Anna
Kozlowski, Cezary A.
[J]. SEPARATION SCIENCE AND TECHNOLOGY, 2016, 51 (14) : 2394 - 2410
[37] Supramolecular calixarene-based catalytic systems in the Wacker-oxidation of higher alkenes
Maksimov, AL
Buchneva, TS
Karakhanov, EA
[J]. JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2004, 217 (1-2) : 59 - 67
[38] Calixarene-Based Surfactants: Conformational-Dependent Solvation Shells for the Alkyl Chains
Basilio, Nuno
Garcia-Rio, Luis
[J]. CHEMPHYSCHEM, 2012, 13 (09) : 2368 - 2376
[39] Calixbenoquin: Calixarene-Based Cluster of Monobenzone as a New Anti-Tyrosinase Agent
Pur, Fazel Nasuhi
[J]. PHARMACEUTICAL CHEMISTRY JOURNAL, 2022, 56 (09) : 1199 - 1202
[40] Calixarene-based hyperbranched molecules with an N,S-multidentate ligand core
Mahouachi, M
Kim, Y
Lee, SH
Abidi, R
Harrowfield, J
Vicens, J
[J]. SUPRAMOLECULAR CHEMISTRY, 2005, 17 (04) : 323 - 330

← 1 2 3 4 5 →