Dithienopyrrole as a Rigid Alternative to the Bithiophene π Relay in Chromophores with Second‐Order Nonlinear Optical Properties. Issue 1 (7th October 2014)
- Record Type:
- Journal Article
- Title:
- Dithienopyrrole as a Rigid Alternative to the Bithiophene π Relay in Chromophores with Second‐Order Nonlinear Optical Properties. Issue 1 (7th October 2014)
- Main Title:
- Dithienopyrrole as a Rigid Alternative to the Bithiophene π Relay in Chromophores with Second‐Order Nonlinear Optical Properties
- Authors:
- Marco, A. Belén
Martínez de Baroja, Natalia
Franco, Santiago
Garín, Javier
Orduna, Jesús
Villacampa, Belén
Revuelto, Alejandro
Andreu, Raquel - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>4<italic>H</italic>‐Pyranylidene‐containing push‐pull chromophores built around a bithiophene (BT) π relay or a rigidified thiophene‐based unit, namely cyclopenta[1, 2‐<italic>b</italic>:3, 4‐<italic>b</italic>′]dithiophene (CPDT) or dithieno[3, 2‐<italic>b</italic>:2′, 3′‐<italic>d</italic>]pyrrole (DTP), have been synthesized and characterized. The effect of these different relays on the polarization and the second‐order nonlinear optical (NLO) properties has been studied. For the sake of comparison, the corresponding reported dithieno[3, 2‐<italic>b</italic>:2′, 3′‐<italic>d</italic>]thiophene (DTT) derivatives have also been included in the discussion. Replacement of the BT core by a rigidified unit (CPDT, DTP) leads to more polarized systems. Calculated NBO charges and electrochemical measurements show that dithienopyrrole has a remarkable donor character that allows an important charge transfer between the donor and the acceptor. The influence of the rigidification of the BT relay on the NLO responses depends on the acceptor strength. For the weakest acceptor used (thiobarbituric acid), passing from the BT relay to the rigidified units always involves an increase in the <italic>μβ</italic><sub>0</sub> figure of merit. Nevertheless, for the strongest acceptor (2‐dicyanomethylene‐3‐cyano‐4, 5, 5‐trimethyl‐2, 5‐dihydrofuran (TCF)), a slight increase in <italic>μβ</italic><sub>0</sub> with respect to<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>4<italic>H</italic>‐Pyranylidene‐containing push‐pull chromophores built around a bithiophene (BT) π relay or a rigidified thiophene‐based unit, namely cyclopenta[1, 2‐<italic>b</italic>:3, 4‐<italic>b</italic>′]dithiophene (CPDT) or dithieno[3, 2‐<italic>b</italic>:2′, 3′‐<italic>d</italic>]pyrrole (DTP), have been synthesized and characterized. The effect of these different relays on the polarization and the second‐order nonlinear optical (NLO) properties has been studied. For the sake of comparison, the corresponding reported dithieno[3, 2‐<italic>b</italic>:2′, 3′‐<italic>d</italic>]thiophene (DTT) derivatives have also been included in the discussion. Replacement of the BT core by a rigidified unit (CPDT, DTP) leads to more polarized systems. Calculated NBO charges and electrochemical measurements show that dithienopyrrole has a remarkable donor character that allows an important charge transfer between the donor and the acceptor. The influence of the rigidification of the BT relay on the NLO responses depends on the acceptor strength. For the weakest acceptor used (thiobarbituric acid), passing from the BT relay to the rigidified units always involves an increase in the <italic>μβ</italic><sub>0</sub> figure of merit. Nevertheless, for the strongest acceptor (2‐dicyanomethylene‐3‐cyano‐4, 5, 5‐trimethyl‐2, 5‐dihydrofuran (TCF)), a slight increase in <italic>μβ</italic><sub>0</sub> with respect to the BT chromophore is only observed for the DTP derivative. Thus, rigidification of the BT core is not enough to improve the second‐order nonlinearity and the incorporation of a DTP moiety has proven to be the most efficient approach for this purpose.</p> </abstract> … (more)
- Is Part Of:
- Chemistry, an Asian journal. Volume 10:Issue 1(2015:Jan.)
- Journal:
- Chemistry, an Asian journal
- Issue:
- Volume 10:Issue 1(2015:Jan.)
- Issue Display:
- Volume 10, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 10
- Issue:
- 1
- Issue Sort Value:
- 2015-0010-0001-0000
- Page Start:
- 188
- Page End:
- 197
- Publication Date:
- 2014-10-07
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X ↗
http://www3.interscience.wiley.com/journal/112140232/home ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/asia.201402870 ↗
- Languages:
- English
- ISSNs:
- 1861-4728
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4133.xml