Abstract
Exacting control over conformation in response to an external stimulus is the central focus of molecular switching. Here we describe the synthesis of a series of diphenylacetylene-based molecular switches, and examine their response to covalent modification and deprotonation at remote phenolic positions. A complex interplay between multiple intramolecular hydrogen bond donors and acceptors determines the global conformation.
| Original language | English |
|---|---|
| Pages (from-to) | 9384-9388 |
| Number of pages | 5 |
| Journal | Organic and Biomolecular Chemistry |
| Volume | 12 |
| Issue number | 46 |
| Early online date | 08 Oct 2014 |
| DOIs | |
| Publication status | Published - 2014 |
| Externally published | Yes |
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Organic Chemistry
- Biochemistry
- General Medicine
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