2007
DOI: 10.1016/j.optcom.2006.10.020
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Third order optical nonlinearities of eight-β-octa-octyloxy-phthalocyanines

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Cited by 12 publications
(5 citation statements)
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“…Further, the Q-band shows a well defined split in the case of ClNf whereas it is unsplit in the case of ClSNf. This is in agreement with earlier observations that the metal ion gets expelled from the molecule during its incorporation in Nafion, and it gets embedded in the free base form. , The split in the Q-band spectrum of ClNf shown here resembles that reported in the case of the free base of a very similar compound which was attributed to the lowering in symmetry . Bare solid Nafion contains hydrophilic/hydrophobic domains distributed in indistinguishable manner, at random.…”
Section: Resultssupporting
confidence: 92%
See 1 more Smart Citation
“…Further, the Q-band shows a well defined split in the case of ClNf whereas it is unsplit in the case of ClSNf. This is in agreement with earlier observations that the metal ion gets expelled from the molecule during its incorporation in Nafion, and it gets embedded in the free base form. , The split in the Q-band spectrum of ClNf shown here resembles that reported in the case of the free base of a very similar compound which was attributed to the lowering in symmetry . Bare solid Nafion contains hydrophilic/hydrophobic domains distributed in indistinguishable manner, at random.…”
Section: Resultssupporting
confidence: 92%
“…3,36 The split in the Q-band spectrum of ClNf shown here resembles that reported in the case of the free base of a very similar compound which was attributed to the lowering in symmetry. 37 Bare solid Nafion contains hydrophilic/hydrophobic domains distributed in indistinguishable manner, at random. When Nafion is immersed in dye solution, the ClAlPc is expected to localize in the hydrophobic clusters present in structural nanopores of the Nafion membrane.…”
Section: Resultsmentioning
confidence: 99%
“…In fact, the variation of the central atom can introduce significant changes in the NLO behavior as far as OL is concerned. This is especially true in the case of PcMXs with MX = VO, TiO, or InCl. ,,,, The reason for such variations is due to the ability of the central moieties, such as VO, TiO, or InCl, to introduce dipole moments perpendicularly oriented to the Pc ring with values in the order of 10–15 D, which alter the electronic structure of the macrocycle in both ground and excited states, and provoke new steric effects that modify the aggregation of PcMXs. , …”
Section: Phthalocyanines and Related Macrocyclesmentioning
confidence: 99%
“…[1][2][3] Among the organic based NLO materials concerned, phthalocyanines and their derivatives are attracting much more intensive research attention in the development of nonlinear optical materials because their highly delocalized π-electron conjugated macrocyclic systems can be highly polarized under a photovoltaic field and consequently result in large nonlinear optical responses with a fast response speed, low optical damage threshold, and a small dielectric constant. [4][5][6][7] After extensive studies conducted on simple monomeric phthalocyanine systems in the early stages, it is realized that improved optical nonlinearities of phthalocyanines can be achieved in phthalocyanine nanoparticles, 8 J-aggregates, 9 hybrid-glass composites, 10 mesogenic systems, 11 metallophthalocyanines, 12 octasubstituted metallophthalocyanines, 13 bis-phthalocyanines and so on. 5,14,15 Later on special attention was given to push-pull (asymmetrically) phthalocyanines where the conjugated π-electron system is separated/enhanced by different donor or acceptor groups.…”
Section: Introductionmentioning
confidence: 99%