Macrocyclic Hamilton-type receptors comprising a ferrocene pivot

Luca Pisciottani; Maxime Douarre; Brigitte Bibal; Clotilde Davies; Holly Roberts; Brice Kauffmann; Sarah L. Horswell; James H.R. Tucker; Nathan D. McClenaghan

doi:10.1080/10610278.2018.1426856

Macrocyclic Hamilton-type receptors comprising a ferrocene pivot

Luca Pisciottani, Maxime Douarre, Brigitte Bibal, Clotilde Davies, Holly Roberts, Brice Kauffmann, Sarah L. Horswell, James H.R. Tucker, Nathan D. McClenaghan^*

^*Corresponding author for this work

Chemistry

Research output: Contribution to journal › Article › peer-review

4 Citations (Scopus)

Abstract

Synthetic hydrogen-bonding receptors are described, which incorporate a central electroactive ferrocene moiety grafted with two adjacent bis(amido)pyridine motifs and an aliphatic tether (14 and 18 methylene units for 1 and 2, respectively) completing the macrocycle. The crystallographic structure, barbiturate guest-binding studies and electrochemical data are provided for the more strongly-binding macrocycle 2.

Original language	English
Pages (from-to)	869-875
Number of pages	7
Journal	Supramolecular Chemistry
Volume	30
Issue number	10
Early online date	17 Jan 2018
DOIs	https://doi.org/10.1080/10610278.2018.1426856
Publication status	Published - 3 Oct 2018

Keywords

barbiturate
ferrocene
Hamilton receptor
hydrogen-bonding
Macrocycle

ASJC Scopus subject areas

General Chemistry

Access to Document

10.1080/10610278.2018.1426856

Cite this

@article{80bcf3c1b26046488d64a85ea742e481,

title = "Macrocyclic Hamilton-type receptors comprising a ferrocene pivot",

abstract = "Synthetic hydrogen-bonding receptors are described, which incorporate a central electroactive ferrocene moiety grafted with two adjacent bis(amido)pyridine motifs and an aliphatic tether (14 and 18 methylene units for 1 and 2, respectively) completing the macrocycle. The crystallographic structure, barbiturate guest-binding studies and electrochemical data are provided for the more strongly-binding macrocycle 2.",

keywords = "barbiturate, ferrocene, Hamilton receptor, hydrogen-bonding, Macrocycle",

author = "Luca Pisciottani and Maxime Douarre and Brigitte Bibal and Clotilde Davies and Holly Roberts and Brice Kauffmann and Horswell, {Sarah L.} and Tucker, {James H.R.} and McClenaghan, {Nathan D.}",

year = "2018",

month = oct,

day = "3",

doi = "10.1080/10610278.2018.1426856",

language = "English",

volume = "30",

pages = "869--875",

journal = "Supramolecular Chemistry",

issn = "1061-0278",

publisher = "Taylor & Francis",

number = "10",

}

TY - JOUR

T1 - Macrocyclic Hamilton-type receptors comprising a ferrocene pivot

AU - Pisciottani, Luca

AU - Douarre, Maxime

AU - Bibal, Brigitte

AU - Davies, Clotilde

AU - Roberts, Holly

AU - Kauffmann, Brice

AU - Horswell, Sarah L.

AU - Tucker, James H.R.

AU - McClenaghan, Nathan D.

PY - 2018/10/3

Y1 - 2018/10/3

N2 - Synthetic hydrogen-bonding receptors are described, which incorporate a central electroactive ferrocene moiety grafted with two adjacent bis(amido)pyridine motifs and an aliphatic tether (14 and 18 methylene units for 1 and 2, respectively) completing the macrocycle. The crystallographic structure, barbiturate guest-binding studies and electrochemical data are provided for the more strongly-binding macrocycle 2.

AB - Synthetic hydrogen-bonding receptors are described, which incorporate a central electroactive ferrocene moiety grafted with two adjacent bis(amido)pyridine motifs and an aliphatic tether (14 and 18 methylene units for 1 and 2, respectively) completing the macrocycle. The crystallographic structure, barbiturate guest-binding studies and electrochemical data are provided for the more strongly-binding macrocycle 2.

KW - barbiturate

KW - ferrocene

KW - Hamilton receptor

KW - hydrogen-bonding

KW - Macrocycle

UR - http://www.scopus.com/inward/record.url?scp=85041011330&partnerID=8YFLogxK

U2 - 10.1080/10610278.2018.1426856

DO - 10.1080/10610278.2018.1426856

M3 - Article

AN - SCOPUS:85041011330

SN - 1061-0278

VL - 30

SP - 869

EP - 875

JO - Supramolecular Chemistry

JF - Supramolecular Chemistry

IS - 10

ER -

Macrocyclic Hamilton-type receptors comprising a ferrocene pivot

Abstract

Keywords

ASJC Scopus subject areas

Access to Document

Fingerprint

Cite this