期刊
RSC ADVANCES
卷 7, 期 22, 页码 13232-13239出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c6ra27176f
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资金
- New Zealand Ministry of Business, Innovation and Employment [UOAX1202]
- New Zealand Ministry of Business, Innovation & Employment (MBIE) [UOAX1202] Funding Source: New Zealand Ministry of Business, Innovation & Employment (MBIE)
A series of multi-branched two-photon photoinitiators (PIs) based around the well-known triphenylamine donor core were synthesised for use in two-photon polymerisation (TPP) and are designated as compounds 6, 7 and 8. The use of a phenylene-vinylene pi-system was used with an ethyl ester acceptor moiety which gives dipolar (6), quadrupolar (7) and octupolar (8) branching. Two-photon absorption cross-sections (delta(2PA)) of 126 GM, 358 GM and 590 GM were measured at 780 nm for 6, 7 and 8, respectively. The fluorescence quantum yields (phi(F)) were determined in both MeOH and the acrylate system employed for TPP, and demonstrate the impact of viscosity upon photophysical properties of multi-branched molecules. Excellent polymerisation thresholds were demonstrated in the mW region: namely 45 mu W (6), 61 mu W (7) and 27 mu W (8) at a writing speed of 50 mu m s(-1). Finally, an explanation for the disparity of polymerisation thresholds is proposed for these PIs and provides insight into the future development of low threshold PIs for TPP.
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