Sulfoxide‐Induced Homochiral Folding of ortho‐Phenylene Ethynylenes (o‐OPEs) by Silver(I) Templating: Structure and Chiroptical Properties. Issue 11 (24th January 2018)
- Record Type:
- Journal Article
- Title:
- Sulfoxide‐Induced Homochiral Folding of ortho‐Phenylene Ethynylenes (o‐OPEs) by Silver(I) Templating: Structure and Chiroptical Properties. Issue 11 (24th January 2018)
- Main Title:
- Sulfoxide‐Induced Homochiral Folding of ortho‐Phenylene Ethynylenes (o‐OPEs) by Silver(I) Templating: Structure and Chiroptical Properties
- Authors:
- Resa, Sandra
Miguel, Delia
Guisán‐Ceinos, Santiago
Mazzeo, Giuseppe
Choquesillo‐Lazarte, Duane
Abbate, Sergio
Crovetto, Luis
Cárdenas, Diego J.
Carreño, M. Carmen
Ribagorda, María
Longhi, Giovanna
Mota, Antonio J.
Álvarez de Cienfuegos, Luis
Cuerva, Juan M. - Abstract:
- Abstract: A new family of homochiral silver complexes based on carbophilic interactions with ortho ‐phenylene ethynylene ( o ‐OPE) scaffolds containing up to two silver atoms are described. These compounds represent a unique class of complexes with chirality at the metal. Chiral induction is based on the inclusion of chiral sulfoxides, which allow efficient transfer of chirality to the helically folded o ‐OPE, leading to circularly polarized luminescence (CPL)‐ and vibrational circular dichroism (VCD)‐active compounds. In the presence of silver(I) cations, carbophilic interactions dominate, which promote helical structures with a defined helicity. This is one of the very scarce examples of the use of such interactions in the attractive field of abiotic foldamers. The switching event has been extensively studied by using different chiroptical techniques, including circular dichroism, CPL, and VCD, and represents one of the few CPL switches described in the literature. Abstract : Silver twists : A new family of homochiral silver complexes based on carbophilic interactions with ortho ‐phenylene ethynylene ( o ‐OPE) scaffolds containing up to two silver atoms are described. In the presence of silver(I) cations, carbophilic interactions dominate, which promote helical structures with a defined helicity (see figure). This is one of the very scarce examples of the use of such interactions in the attractive field of abiotic foldamers.
- Is Part Of:
- Chemistry. Volume 24:Issue 11(2018)
- Journal:
- Chemistry
- Issue:
- Volume 24:Issue 11(2018)
- Issue Display:
- Volume 24, Issue 11 (2018)
- Year:
- 2018
- Volume:
- 24
- Issue:
- 11
- Issue Sort Value:
- 2018-0024-0011-0000
- Page Start:
- 2653
- Page End:
- 2662
- Publication Date:
- 2018-01-24
- Subjects:
- chiroptical properties -- helical structures -- host–guest systems -- nanostructures -- supramolecular chemistry
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201704897 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 5904.xml