ORCID Profile
0000-0002-5404-2455
Current Organisation
Wroclaw University of Science and Technology
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Publisher: CSIRO Publishing
Date: 2012
DOI: 10.1071/CH12054
Abstract: The alkynes HC≡CC6H2-2,6-Et2-4-C≡CC6H4-4-NO2 (4) and HC≡CC6H4-4-C≡CC6H2-2,6-Et2-4-C≡CC6H4-4-NO2 (6) and gold alkynyl complexes Au{C≡CC6H2-2,5-(OEt)2-4-C≡CC6H4-4-NO2}(PPh3) (7), Au(C≡CC6H2-2,6-Et2-4-C≡CC6H4-4-NO2)(PPh3) (8), and Au(C≡CC6H4-4-C≡CC6H2-2,6-Et2-4-C≡CC6H4-4-NO2)(PPh3) (9) have been synthesized. The linear optical properties and quadratic optical non-linearities of 7–9 have been measured, the latter by hyper-Rayleigh scattering at 1064 nm, and compared with data for the previously reported complexes Au(C≡CC6H4-4-NO2)(PPh3) (10) and Au(C≡CC6H4-4-C≡CC6H4-4-NO2)(PPh3) (11). The optical absorption maximum red-shifts and the first hyperpolarizabilities increase on π-system lengthening and on introduction of electron-releasing substituents on the π-bridge ring adjacent to the metal centre. The cubic non-linear optical properties of 1,4-{(PCy3)Au(C≡C)}2C6H4 (12) and {(PCy3)Au(C≡C-4-C6H4C≡C)}6C6 (13) have been assessed by wide spectroscopic range femtosecond Z-scan studies the maximal values of the imaginary component and the effective two-photon absorption cross-section increase markedly on proceeding from linear complex 12 to 6-fold-symmetric complex 13, an increase that is maintained when data are scaled by relative molecular weight.
Publisher: American Chemical Society (ACS)
Date: 04-01-2022
Publisher: Wiley
Date: 31-10-2018
Abstract: Straightforward syntheses of bis[bis{1,2-bis(diphenylphosphino)ethane}ruthenium]-functionalized 1,3,5-triethynylbenzene-cored complexes via a methodology employing "steric control" permit facile formation of Y-shaped Sonogashira coupling products and distorted-H-shaped homo-coupled quadrupolar products. Cyclic voltammetric data from these products reveal two reversible metal alkynyl-localized oxidation processes for all complexes. The wavelengths of the linear optical absorption maxima are dominated by the nature of the peripheral alkynyl ligand rather than the substituent at the unique arm of the "Y" or at the quadrupolar complex "core". The quadratic optical nonlinearities of the Y-shaped complexes were assessed by the hyper-Rayleigh scattering technique at 800 nm and employing 100 fs light pulses introduction of donor NEt
Publisher: Wiley
Date: 19-05-2015
Publisher: Wiley
Date: 02-2012
Abstract: Ruthenium alkynyl dendrimers up to second generation in size have been prepared by a ergent route and exploiting Sonogashira coupling. The cubic NLO properties have been examined by wide spectral range fs Z‐scan studies, revealing an NLO dendritic effect. The significant increase in NLO properties seen on generation increase is maintained when the coefficients are scaled by the number of metal atoms, the dendrimer molecular weights, or the number of “effective” (delocalizable π) electrons in the dendritic structures.
Publisher: The Optical Society
Date: 05-08-2013
DOI: 10.1364/OL.38.002945
Publisher: Elsevier BV
Date: 12-2012
Publisher: Royal Society of Chemistry (RSC)
Date: 2021
DOI: 10.1039/D1CP03346H
Abstract: The structural and electronic factors influencing their two-photon absorption cross-sections of nine TCBD derivatives are discussed.
Publisher: Wiley
Date: 14-06-2016
Abstract: The synthesis and characterization of four new tetracyanobutadiene (TCBD) derivatives (1-3 and 2') incorporating 2- or 2,7-fluorenyl and diphenylamino moieties are reported. The electroactivity of 1-3 and 2' was studied by cyclic voltammetry (CV), while the linear optical and (third-order) nonlinear optical (NLO) properties were investigated by electronic spectroscopy and Z-scan studies, respectively. All experimental investigations were rationalized by DFT computations, providing an insight into the electronic structure of these derivatives and on their application potential. We show that these derivatives are nonluminescent in solution at ambient temperatures, but become fluorescent in solvent glasses. This finding constitutes an unprecedented observation for TCBD derivatives. Also, we show by Z-scan studies that these derivatives behave as two-photon absorbers in the near-IR range (800-1050 nm). These third-order NLO properties are discussed and compared with those of their alkynyl precursors (4-6), which have been investigated by two-photon excited fluorescence (TPEF).
Publisher: American Chemical Society (ACS)
Date: 03-12-2014
DOI: 10.1021/LA504558Z
Publisher: Elsevier BV
Date: 11-2011
Publisher: Wiley
Date: 31-10-2018
Publisher: Wiley
Date: 04-02-2011
Publisher: Royal Society of Chemistry (RSC)
Date: 2016
DOI: 10.1039/C6CC02560A
Abstract: End-functionalization of OPVs by chlorobis{bis(diphenylphosphino)ethane}ruthenium alkynyl units affords molecules with exceptionally large two- and three-photon absorption cross-sections.
Publisher: Royal Society of Chemistry (RSC)
Date: 2015
DOI: 10.1039/C5RA08302H
Abstract: We report on the photophysical and optical properties of a polyfluorene derivative (PFO) and its binding to the amyloid-forming protein insulin.
Publisher: Wiley
Date: 03-07-2015
Abstract: The syntheses of trans-[Ru(C≡CC
Publisher: Wiley
Date: 14-04-2011
Abstract: The new [(η(2)-dppe)(η(5)-C(5)Me(5))Fe(C≡C-1,4-C(6)H(4)C≡C)Ru(η(2) -dppe)(2) C≡C(C(6)H(5))] complex (3-H) and its hexanuclear relative [{(η(2)-dppe)(η(5)-C(5) Me(5))Fe(C≡C-1,4-C(6)H(4)-C≡C)Ru(η(2)-dppe)(2)(C≡C-1,4-C(6)H(4)C≡C)(3)(1,3,5-C(6)H(3))] (4) have been synthesized and characterized. The linear and cubic nonlinear optical properties of these compounds in their various redox states have been studied along with those of the analogous complexes [(η(2)-dppe)(η(5)-C(5)Me(5))Fe(C≡C-1,4-C(6)H(4)C≡C)Ru(η(2)-dppe)(2)R][PF(6)](n) (n=0-2 R=Cl, 2-Cl R=C≡C(4-C(6)H(4)NO(2)),3-NO(2)). We show that molecules exhibiting large third-order nonlinearities can be obtained by assembling such dinuclear Fe/Ru units around a central 1,3,5-substituted C(6)H(3) core. These data are discussed with a particular emphasis on the large changes in their nonlinear (third-order) optical properties brought about by oxidation. Experimental and computational (DFT) evidence for the electronic structures of these compounds in their various redox states is presented using 3-H(n+) as a prototypical model. Single crystals of this complex in its mono-oxidized state (3-H[PF(6)]) provide the first structural data for such carbon-rich Fe(III) /Ru(II) heteronuclear mixed-valent (MV) systems. Although experimental evidence for the structure of the dioxidized states was more difficult to obtain, the theoretical study reveals that 3-H(2+) can be considered to have a biradical structure with two independent spins. The low-lying absorptions that appear in the near-infrared (NIR) range for all these compounds following oxidation correspond to intervalence charge-transfer (IVCT) bands for the mono-oxidized states and to ligand-to-metal charge-transfer (LMCT) transitions for the dioxidized states. These play a crucial role in the strong optical modulation achieved. The possibility of accessing additional states with distinct linear or nonlinear optical properties is also briefly discussed.
Publisher: Royal Society of Chemistry (RSC)
Date: 2012
DOI: 10.1039/C2NJ40589J
Publisher: American Chemical Society (ACS)
Date: 03-11-2015
Publisher: CSIRO Publishing
Date: 2011
DOI: 10.1071/CH11191
Abstract: The cubic hyperpolarizabilities of 1,3,5-(trans-[RuCl(dppe)2(C≡CC6H4-4-C≡C)])3C6H3 (1), 1,3,5-(trans-[Ru(C≡CPh)(dppe)2(C≡CC6H4-4-C≡C)])3C6H3 (2), 1,3,5-(trans-[Ru(C≡CC6H4-4-NO2)(dppe)2(C≡CC6H4-4-C≡C)])3C6H3 (3), 1,3,5-{trans-[Ru(C≡C-3,5-(trans-[Ru(C≡CPh)(dppe)2(C≡CC6H4-4-C≡C)])2C6H3)(dppe)2(C≡CC6H4-4-C≡C)]}3C6H3 (4), and 1,3,5-{trans-[Ru(C≡C-3,5-(trans-[Ru(C≡CC6H4-4-NO2)(dppe)2(C≡CC6H4-4-C≡C)])2C6H3)(dppe)2(C≡CC6H4-4-C≡C)]}3C6H3 (5) have been assessed over the spectral range 520–1600 nm using the Z-scan technique and ~150 fs pulses. All complexes exhibit negative values of γreal (corresponding to self-defocusing behaviour) and significant positive values of γimag (corresponding to two-photon absorption) at short wavelengths (up to 1000 nm). The maximal values of γreal and γimag increase in magnitude on dendrimer generation increase (proceeding from 2 to 4 or 3 to 5). The open-aperture Z-scan results have been used to confirm and contrast the two-photon (2PA) and three-photon absorption (3PA) behaviour of 1–5, the data being consistent with the existence of 2PA at the short wavelength range, but with significant 3PA at longer wavelengths for 1–3 and 5, a record 3PA coefficient for an inorganic complex for 5 at 1180 nm, and appreciable 3PA at the telecommunications wavelength of 1300 nm.
No related grants have been discovered for Marek Samoc.