Hemicucurbit[n]urils

Publikation: Bidrag til bog/antologi/rapport › Bidrag til bog/antologi › Forskning › fagfællebedømt

Standard

Hemicucurbit[n]urils. / Lisbjerg, Micke; Pittelkow, Michael.

Reference Module in Chemistry, Molecular Sciences and Chemical Engineering: Comprehensive Supramolecular Chemistry II. Bind 3 Elsevier, 2017. s. 221-236.

Publikation: Bidrag til bog/antologi/rapport › Bidrag til bog/antologi › Forskning › fagfællebedømt

Harvard

Lisbjerg, M & Pittelkow, M 2017, Hemicucurbit[n]urils. i Reference Module in Chemistry, Molecular Sciences and Chemical Engineering: Comprehensive Supramolecular Chemistry II. bind 3, Elsevier, s. 221-236. https://doi.org/10.1016/B978-0-12-409547-2.12515-6

APA

Lisbjerg, M., & Pittelkow, M. (2017). Hemicucurbit[n]urils. I Reference Module in Chemistry, Molecular Sciences and Chemical Engineering: Comprehensive Supramolecular Chemistry II (Bind 3, s. 221-236). Elsevier. https://doi.org/10.1016/B978-0-12-409547-2.12515-6

Vancouver

Lisbjerg M, Pittelkow M. Hemicucurbit[n]urils. I Reference Module in Chemistry, Molecular Sciences and Chemical Engineering: Comprehensive Supramolecular Chemistry II. Bind 3. Elsevier. 2017. s. 221-236 https://doi.org/10.1016/B978-0-12-409547-2.12515-6

Author

Lisbjerg, Micke ; Pittelkow, Michael. / Hemicucurbit[n]urils. Reference Module in Chemistry, Molecular Sciences and Chemical Engineering: Comprehensive Supramolecular Chemistry II. Bind 3 Elsevier, 2017. s. 221-236

Bibtex

@inbook{a3e91a2fb2454ea9ab67c7061a43df71,
title = "Hemicucurbit[n]urils",
abstract = "Since the discovery of the first hemicucurbit[n]uril macrocycles in 2004, a series of functional hemicucurbit[n]uril derivatives have been prepared and studies of their supramolecular chemistry have been conducted. The original hemicucurbit[n]urils (hemicucurbit[6]uril and hemicucurbit[12]uril) are only sparsely soluble, which hampered studies of their properties as potential hosts in supramolecular chemistry. Recently, a range of homologues have been synthesized (eg, the biotin[n]urils, the bambus[n]urils, and the cyclohexylhemicucurbit[n]urils) that are functionalizable and their supramolecular chemistry has been studied in a range of solvents. This has expanded the scope, and the interest in these structures is growing. In contrast to the more widely studied cucurbit[n]urils that are excellent hosts for cations, the hemicucurbit[n]urils act as hosts for anions. This article provides a comprehensive survey of the literature covering the syntheses of the homologs and derivatives, and their supramolecular chemistry",
author = "Micke Lisbjerg and Michael Pittelkow",
year = "2017",
doi = "10.1016/B978-0-12-409547-2.12515-6",
language = "English",
isbn = "978-0-12-409547-2",
volume = "3",
pages = "221--236",
booktitle = "Reference Module in Chemistry, Molecular Sciences and Chemical Engineering",
publisher = "Elsevier",
address = "Netherlands",

}

RIS

TY - CHAP

T1 - Hemicucurbit[n]urils

AU - Lisbjerg, Micke

AU - Pittelkow, Michael

PY - 2017

Y1 - 2017

N2 - Since the discovery of the first hemicucurbit[n]uril macrocycles in 2004, a series of functional hemicucurbit[n]uril derivatives have been prepared and studies of their supramolecular chemistry have been conducted. The original hemicucurbit[n]urils (hemicucurbit[6]uril and hemicucurbit[12]uril) are only sparsely soluble, which hampered studies of their properties as potential hosts in supramolecular chemistry. Recently, a range of homologues have been synthesized (eg, the biotin[n]urils, the bambus[n]urils, and the cyclohexylhemicucurbit[n]urils) that are functionalizable and their supramolecular chemistry has been studied in a range of solvents. This has expanded the scope, and the interest in these structures is growing. In contrast to the more widely studied cucurbit[n]urils that are excellent hosts for cations, the hemicucurbit[n]urils act as hosts for anions. This article provides a comprehensive survey of the literature covering the syntheses of the homologs and derivatives, and their supramolecular chemistry

AB - Since the discovery of the first hemicucurbit[n]uril macrocycles in 2004, a series of functional hemicucurbit[n]uril derivatives have been prepared and studies of their supramolecular chemistry have been conducted. The original hemicucurbit[n]urils (hemicucurbit[6]uril and hemicucurbit[12]uril) are only sparsely soluble, which hampered studies of their properties as potential hosts in supramolecular chemistry. Recently, a range of homologues have been synthesized (eg, the biotin[n]urils, the bambus[n]urils, and the cyclohexylhemicucurbit[n]urils) that are functionalizable and their supramolecular chemistry has been studied in a range of solvents. This has expanded the scope, and the interest in these structures is growing. In contrast to the more widely studied cucurbit[n]urils that are excellent hosts for cations, the hemicucurbit[n]urils act as hosts for anions. This article provides a comprehensive survey of the literature covering the syntheses of the homologs and derivatives, and their supramolecular chemistry

U2 - 10.1016/B978-0-12-409547-2.12515-6

DO - 10.1016/B978-0-12-409547-2.12515-6

M3 - Book chapter

SN - 978-0-12-409547-2

VL - 3

SP - 221

EP - 236

BT - Reference Module in Chemistry, Molecular Sciences and Chemical Engineering

PB - Elsevier

ER -

ID: 176334729