Fluorination as a route towards unlocking the hydrogen bond donor ability of phenolic compounds in self-assembled monolayers

Harry Pinfold; Graham Pattison; Giovanni Costantini

doi:10.1039/D0CE00213E

Fluorination as a route towards unlocking the hydrogen bond donor ability of phenolic compounds in self-assembled monolayers

Harry Pinfold
, Graham Pattison
, Giovanni Costantini

Applied Chemical Sciences Research Excellence Group

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

Abstract

We report on the comparative performance of a simple diphenol and its fluorinated analogue as hydrogen-bond-donating building blocks for the formation of multicomponent self-assembled monolayers. The fluorinated molecule is found to be a significantly more effective building block than its unfluorinated counterpart.

Original language	English
Pages (from-to)	2425-2428
Number of pages	4
Journal	CrystEngComm
Volume	22
Issue number	14
DOIs	https://doi.org/10.1039/D0CE00213E
Publication status	Published - 12 Mar 2020

Access to Document

10.1039/D0CE00213E

Fluorination as a route towards unlocking the hydrogen bond donor ability of phenolic compounds in self-assembled monolayersAccepted author manuscript, 506 KB

Cite this

@article{5e09101c99b14916a726ebf207dc9622,

title = "Fluorination as a route towards unlocking the hydrogen bond donor ability of phenolic compounds in self-assembled monolayers",

abstract = "We report on the comparative performance of a simple diphenol and its fluorinated analogue as hydrogen-bond-donating building blocks for the formation of multicomponent self-assembled monolayers. The fluorinated molecule is found to be a significantly more effective building block than its unfluorinated counterpart.",

author = "Harry Pinfold and Graham Pattison and Giovanni Costantini",

year = "2020",

month = mar,

day = "12",

doi = "10.1039/D0CE00213E",

language = "English",

volume = "22",

pages = "2425--2428",

journal = "CrystEngComm",

publisher = "Royal Society of Chemistry",

number = "14",

}

TY - JOUR

T1 - Fluorination as a route towards unlocking the hydrogen bond donor ability of phenolic compounds in self-assembled monolayers

AU - Pinfold, Harry

AU - Pattison, Graham

AU - Costantini, Giovanni

PY - 2020/3/12

Y1 - 2020/3/12

N2 - We report on the comparative performance of a simple diphenol and its fluorinated analogue as hydrogen-bond-donating building blocks for the formation of multicomponent self-assembled monolayers. The fluorinated molecule is found to be a significantly more effective building block than its unfluorinated counterpart.

AB - We report on the comparative performance of a simple diphenol and its fluorinated analogue as hydrogen-bond-donating building blocks for the formation of multicomponent self-assembled monolayers. The fluorinated molecule is found to be a significantly more effective building block than its unfluorinated counterpart.

UR - https://www.scopus.com/pages/publications/85083096933

U2 - 10.1039/D0CE00213E

DO - 10.1039/D0CE00213E

M3 - Article

VL - 22

SP - 2425

EP - 2428

JO - CrystEngComm

JF - CrystEngComm

IS - 14

ER -

Fluorination as a route towards unlocking the hydrogen bond donor ability of phenolic compounds in self-assembled monolayers

Abstract

Access to Document

Other files and links

Fingerprint

Cite this