Design of organic molecules with large two-photon absorption cross sections
- PMID: 9733507
- DOI: 10.1126/science.281.5383.1653
Design of organic molecules with large two-photon absorption cross sections
Abstract
A strategy for the design of molecules with large two-photon absorption cross sections, delta, was developed, on the basis of the concept that symmetric charge transfer, from the ends of a conjugated system to the middle, or vice versa, upon excitation is correlated to enhanced values of delta. Synthesized bis(styryl)benzene derivatives with donor-pi-donor, donor-acceptor-donor, and acceptor-donor-acceptor structural motifs exhibit exceptionally large values of delta, up to about 400 times that of trans-stilbene. Quantum chemical calculations performed on these molecules indicate that substantial symmetric charge redistribution occurs upon excitation and provide delta values in good agreement with experimental values. The combination of large delta and high fluorescence quantum yield or triplet yield exhibited by molecules developed here offers potential for unprecedented brightness in two-photon fluorescent imaging or enhanced photosensitivity in two-photon sensitization, respectively.
Similar articles
-
Carborane enhanced two-photon absorption of tribranched fluorophores for fluorescence microscopy imaging.Chem Commun (Camb). 2013 Nov 21;49(90):10638-40. doi: 10.1039/c3cc46276e. Chem Commun (Camb). 2013. PMID: 24096285
-
Theoretical study of two-photon absorption properties and up-conversion efficiency of new symmetric organic π-conjugated molecules for photovoltaic devices.J Mol Model. 2012 Aug;18(8):3657-67. doi: 10.1007/s00894-012-1378-3. Epub 2012 Feb 23. J Mol Model. 2012. PMID: 22358392
-
Enhanced emission and two-photon absorption cross-section by nanoaggregation of a cyano-substituted stilbene derivative.J Nanosci Nanotechnol. 2008 Sep;8(9):4793-6. doi: 10.1166/jnn.2008.ic71. J Nanosci Nanotechnol. 2008. PMID: 19049110
-
Tandem Systems for Two-Photon Uncaging of Bioactive Molecules.Chempluschem. 2019 Jun;84(6):589-598. doi: 10.1002/cplu.201900139. Epub 2019 May 13. Chempluschem. 2019. PMID: 31944026 Review.
-
Dipyrrolonaphthyridinedione - (still) a mysterious cross-conjugated chromophore.Chem Sci. 2023 Nov 10;14(48):14020-14038. doi: 10.1039/d3sc05272a. eCollection 2023 Dec 13. Chem Sci. 2023. PMID: 38098709 Free PMC article. Review.
Cited by
-
Two-photon polymerization for 3D biomedical scaffolds: Overview and updates.Front Bioeng Biotechnol. 2022 Aug 22;10:994355. doi: 10.3389/fbioe.2022.994355. eCollection 2022. Front Bioeng Biotechnol. 2022. PMID: 36072288 Free PMC article. Review.
-
The mechanism of benzothiazole styrylcyanine dyes binding with dsDNA: studies by spectral-luminescent methods.J Fluoresc. 2008 Jan;18(1):139-47. doi: 10.1007/s10895-007-0252-7. Epub 2007 Sep 28. J Fluoresc. 2008. PMID: 17902039
-
Synthesis and Emergent Photophysical Properties of Diketopyrrolopyrrole-Based Supramolecular Self-Assembly.ACS Omega. 2022 Jun 30;7(27):23179-23188. doi: 10.1021/acsomega.2c01091. eCollection 2022 Jul 12. ACS Omega. 2022. PMID: 35847286 Free PMC article.
-
Triplet excited state properties in variable gap π-conjugated donor-acceptor-donor chromophores.Chem Sci. 2016 Jun 1;7(6):3621-3631. doi: 10.1039/c5sc04578a. Epub 2016 Feb 12. Chem Sci. 2016. PMID: 29997854 Free PMC article.
-
Exceptional three- to six-photon absorption at organometallic dendrimers.Chem Sci. 2024 May 14;15(23):8731-8739. doi: 10.1039/d4sc01127a. eCollection 2024 Jun 12. Chem Sci. 2024. PMID: 38873073 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous