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Photoisomerization of the cyanoacrylic acid acceptor group--a potential problem for organic dyes in solar cells.

Physical chemistry chemical physics : PCCP

Zietz B, Gabrielsson E, Johansson V, El-Zohry AM, Sun L, Kloo L.
PMID: 24382585
Phys Chem Chem Phys. 2014 Feb 14;16(6):2251-5. doi: 10.1039/c3cp54048k.

Organic solar cell dyes containing the most common anchoring group, cyanoacrylic acid, are shown to be photolabile and undergo photoisomerization. This may have significant consequences for dye-sensitized solar cells, as isomerisation competes with electron injection and leads to modifications...

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Zietz B, Gabrielsson E, Johansson V, et al. Photoisomerization of the cyanoacrylic acid acceptor group--a potential problem for organic dyes in solar cells. Phys Chem Chem Phys. 2014;16(6):2251-5doi: 10.1039/c3cp54048k.
Zietz, B., Gabrielsson, E., Johansson, V., El-Zohry, A. M., Sun, L., & Kloo, L. (2014). Photoisomerization of the cyanoacrylic acid acceptor group--a potential problem for organic dyes in solar cells. Physical chemistry chemical physics : PCCP, 16(6), 2251-5. https://doi.org/10.1039/c3cp54048k
Zietz, Burkhard, et al. "Photoisomerization of the cyanoacrylic acid acceptor group--a potential problem for organic dyes in solar cells." Physical chemistry chemical physics : PCCP vol. 16,6 (2014): 2251-5. doi: https://doi.org/10.1039/c3cp54048k
Zietz B, Gabrielsson E, Johansson V, El-Zohry AM, Sun L, Kloo L. Photoisomerization of the cyanoacrylic acid acceptor group--a potential problem for organic dyes in solar cells. Phys Chem Chem Phys. 2014 Feb 14;16(6):2251-5. doi: 10.1039/c3cp54048k. PMID: 24382585.
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Electronic plants.

Science advances

Stavrinidou E, Gabrielsson R, Gomez E, Crispin X, Nilsson O, Simon DT, Berggren M.
PMID: 26702448
Sci Adv. 2015 Nov 20;1(10):e1501136. doi: 10.1126/sciadv.1501136. eCollection 2015 Nov.

The roots, stems, leaves, and vascular circuitry of higher plants are responsible for conveying the chemical signals that regulate growth and functions. From a certain perspective, these features are analogous to the contacts, interconnections, devices, and wires of discrete...

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Stavrinidou E, Gabrielsson R, Gomez E, et al. Electronic plants. Sci Adv. 2015;1(10):e1501136doi: 10.1126/sciadv.1501136.
Stavrinidou, E., Gabrielsson, R., Gomez, E., Crispin, X., Nilsson, O., Simon, D. T., & Berggren, M. (2015). Electronic plants. Science advances, 1(10), e1501136. https://doi.org/10.1126/sciadv.1501136
Stavrinidou, Eleni, et al. "Electronic plants." Science advances vol. 1,10 (2015): e1501136. doi: https://doi.org/10.1126/sciadv.1501136
Stavrinidou E, Gabrielsson R, Gomez E, Crispin X, Nilsson O, Simon DT, Berggren M. Electronic plants. Sci Adv. 2015 Nov 20;1(10):e1501136. doi: 10.1126/sciadv.1501136. eCollection 2015 Nov. PMID: 26702448; PMCID: PMC4681328.
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Breast Milk and Solid Food Shaping Intestinal Immunity.

Frontiers in immunology

Parigi SM, Eldh M, Larssen P, Gabrielsson S, Villablanca EJ.
PMID: 26347740
Front Immunol. 2015 Aug 19;6:415. doi: 10.3389/fimmu.2015.00415. eCollection 2015.

After birth, the intestinal immune system enters a critical developmental stage, in which tolerogenic and pro-inflammatory cells emerge to contribute to the overall health of the host. The neonatal health is continuously challenged by microbial colonization and food intake,...

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Parigi SM, Eldh M, Larssen P, et al. Breast Milk and Solid Food Shaping Intestinal Immunity. Front Immunol. 2015;6:415doi: 10.3389/fimmu.2015.00415.
Parigi, S. M., Eldh, M., Larssen, P., Gabrielsson, S., & Villablanca, E. J. (2015). Breast Milk and Solid Food Shaping Intestinal Immunity. Frontiers in immunology, 6415. https://doi.org/10.3389/fimmu.2015.00415
Parigi, Sara M, et al. "Breast Milk and Solid Food Shaping Intestinal Immunity." Frontiers in immunology vol. 6 (2015): 415. doi: https://doi.org/10.3389/fimmu.2015.00415
Parigi SM, Eldh M, Larssen P, Gabrielsson S, Villablanca EJ. Breast Milk and Solid Food Shaping Intestinal Immunity. Front Immunol. 2015 Aug 19;6:415. doi: 10.3389/fimmu.2015.00415. eCollection 2015. PMID: 26347740; PMCID: PMC4541369.
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Thermoelectric Polymers and their Elastic Aerogels.

Advanced materials (Deerfield Beach, Fla.)

Khan ZU, Edberg J, Hamedi MM, Gabrielsson R, Granberg H, Wågberg L, Engquist I, Berggren M, Crispin X.
PMID: 26836440
Adv Mater. 2016 Jun;28(22):4556-62. doi: 10.1002/adma.201505364. Epub 2016 Feb 02.

Electronically conducting polymers constitute an emerging class of materials for novel electronics, such as printed electronics and flexible electronics. Their properties have been further diversified to introduce elasticity, which has opened new possibility for "stretchable" electronics. Recent discoveries demonstrate...

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Khan ZU, Edberg J, Hamedi MM, et al. Thermoelectric Polymers and their Elastic Aerogels. Adv Mater. 2016;28(22):4556-62doi: 10.1002/adma.201505364.
Khan, Z. U., Edberg, J., Hamedi, M. M., Gabrielsson, R., Granberg, H., Wågberg, L., Engquist, I., Berggren, M., & Crispin, X. (2016). Thermoelectric Polymers and their Elastic Aerogels. Advanced materials (Deerfield Beach, Fla.), 28(22), 4556-62. https://doi.org/10.1002/adma.201505364
Khan, Zia Ullah, et al. "Thermoelectric Polymers and their Elastic Aerogels." Advanced materials (Deerfield Beach, Fla.) vol. 28,22 (2016): 4556-62. doi: https://doi.org/10.1002/adma.201505364
Khan ZU, Edberg J, Hamedi MM, Gabrielsson R, Granberg H, Wågberg L, Engquist I, Berggren M, Crispin X. Thermoelectric Polymers and their Elastic Aerogels. Adv Mater. 2016 Jun;28(22):4556-62. doi: 10.1002/adma.201505364. Epub 2016 Feb 02. PMID: 26836440.
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The anti-inflammatory compound palmitoylethanolamide inhibits prostaglandin and hydroxyeicosatetraenoic acid production by a macrophage cell line.

Pharmacology research & perspectives

Gabrielsson L, Gouveia-Figueira S, Häggström J, Alhouayek M, Fowler CJ.
PMID: 28357126
Pharmacol Res Perspect. 2017 Feb 27;5(2):e00300. doi: 10.1002/prp2.300. eCollection 2017 Apr.

The anti-inflammatory agent palmitoylethanolamide (PEA) reduces cyclooxygenase (COX) activity in vivo in a model of inflammatory pain. It is not known whether the compound reduces prostaglandin production in RAW264.7 cells, whether such an action is affected by compounds preventing...

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Gabrielsson L, Gouveia-Figueira S, Häggström J, et al. The anti-inflammatory compound palmitoylethanolamide inhibits prostaglandin and hydroxyeicosatetraenoic acid production by a macrophage cell line. Pharmacol Res Perspect. 2017;5(2):e00300doi: 10.1002/prp2.300.
Gabrielsson, L., Gouveia-Figueira, S., Häggström, J., Alhouayek, M., & Fowler, C. J. (2017). The anti-inflammatory compound palmitoylethanolamide inhibits prostaglandin and hydroxyeicosatetraenoic acid production by a macrophage cell line. Pharmacology research & perspectives, 5(2), e00300. https://doi.org/10.1002/prp2.300
Gabrielsson, Linda, et al. "The anti-inflammatory compound palmitoylethanolamide inhibits prostaglandin and hydroxyeicosatetraenoic acid production by a macrophage cell line." Pharmacology research & perspectives vol. 5,2 (2017): e00300. doi: https://doi.org/10.1002/prp2.300
Gabrielsson L, Gouveia-Figueira S, Häggström J, Alhouayek M, Fowler CJ. The anti-inflammatory compound palmitoylethanolamide inhibits prostaglandin and hydroxyeicosatetraenoic acid production by a macrophage cell line. Pharmacol Res Perspect. 2017 Feb 27;5(2):e00300. doi: 10.1002/prp2.300. eCollection 2017 Apr. PMID: 28357126; PMCID: PMC5368964.
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Electronic structure and excited states of rhenium(I) amido and phosphido carbonyl-bipyridine complexes studied by picosecond time-resolved IR spectroscopy and DFT calculations.

Inorganic chemistry

Gabrielsson A, Busby M, Matousek P, Towrie M, Hevia E, Cuesta L, Perez J, Zális S, Vlcek A.
PMID: 17112276
Inorg Chem. 2006 Nov 27;45(24):9789-97. doi: 10.1021/ic0614768.

UV-vis absorption and picosecond time-resolved IR (TRIR) spectra of amido and phosphido complexes fac-[Re(ER2)(CO)3(bpy)] (ER2 = NHPh, NTol2, PPh2, bpy = 2,2'-bipyridine, Tol = 4-methylphenyl) were investigated in conjunction with DFT and TD-DFT calculations in order to understand their...

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Gabrielsson A, Busby M, Matousek P, et al. Electronic structure and excited states of rhenium(I) amido and phosphido carbonyl-bipyridine complexes studied by picosecond time-resolved IR spectroscopy and DFT calculations. Inorg Chem. 2006;45(24):9789-97doi: 10.1021/ic0614768.
Gabrielsson, A., Busby, M., Matousek, P., Towrie, M., Hevia, E., Cuesta, L., Perez, J., Zális, S., & Vlcek, A. (2006). Electronic structure and excited states of rhenium(I) amido and phosphido carbonyl-bipyridine complexes studied by picosecond time-resolved IR spectroscopy and DFT calculations. Inorganic chemistry, 45(24), 9789-97. https://doi.org/10.1021/ic0614768
Gabrielsson, Anders, et al. "Electronic structure and excited states of rhenium(I) amido and phosphido carbonyl-bipyridine complexes studied by picosecond time-resolved IR spectroscopy and DFT calculations." Inorganic chemistry vol. 45,24 (2006): 9789-97. doi: https://doi.org/10.1021/ic0614768
Gabrielsson A, Busby M, Matousek P, Towrie M, Hevia E, Cuesta L, Perez J, Zális S, Vlcek A. Electronic structure and excited states of rhenium(I) amido and phosphido carbonyl-bipyridine complexes studied by picosecond time-resolved IR spectroscopy and DFT calculations. Inorg Chem. 2006 Nov 27;45(24):9789-97. doi: 10.1021/ic0614768. PMID: 17112276.
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Excited states of nitro-polypyridine metal complexes and their ultrafast decay. Time-resolved IR Absorption, spectroelectrochemistry, and TD-DFT calculations of fac-[Re(Cl)(CO)3(5-nitro-1,10-phenanthroline)].

The journal of physical chemistry. A

Gabrielsson A, Matousek P, Towrie M, Hartl F, Zalis S, Vlcek A.
PMID: 16833954
J Phys Chem A. 2005 Jul 21;109(28):6147-53. doi: 10.1021/jp051677h.

The lowest absorption band of fac-[Re(Cl)(CO)3(5-NO2-phen)] encompasses two close-lying MLCT transitions. The lower one is directed to LUMO, which is heavily localized on the NO2 group. The UV-vis absorption spectrum is well accounted for by TD-DFT (G03/PBEPBE1/CPCM), provided that...

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Gabrielsson A, Matousek P, Towrie M, et al. Excited states of nitro-polypyridine metal complexes and their ultrafast decay. Time-resolved IR Absorption, spectroelectrochemistry, and TD-DFT calculations of fac-[Re(Cl)(CO)3(5-nitro-1,10-phenanthroline)]. J Phys Chem A. 2005;109(28):6147-53doi: 10.1021/jp051677h.
Gabrielsson, A., Matousek, P., Towrie, M., Hartl, F., Zalis, S., & Vlcek, A. (2005). Excited states of nitro-polypyridine metal complexes and their ultrafast decay. Time-resolved IR Absorption, spectroelectrochemistry, and TD-DFT calculations of fac-[Re(Cl)(CO)3(5-nitro-1,10-phenanthroline)]. The journal of physical chemistry. A, 109(28), 6147-53. https://doi.org/10.1021/jp051677h
Gabrielsson, Anders, et al. "Excited states of nitro-polypyridine metal complexes and their ultrafast decay. Time-resolved IR Absorption, spectroelectrochemistry, and TD-DFT calculations of fac-[Re(Cl)(CO)3(5-nitro-1,10-phenanthroline)]." The journal of physical chemistry. A vol. 109,28 (2005): 6147-53. doi: https://doi.org/10.1021/jp051677h
Gabrielsson A, Matousek P, Towrie M, Hartl F, Zalis S, Vlcek A. Excited states of nitro-polypyridine metal complexes and their ultrafast decay. Time-resolved IR Absorption, spectroelectrochemistry, and TD-DFT calculations of fac-[Re(Cl)(CO)3(5-nitro-1,10-phenanthroline)]. J Phys Chem A. 2005 Jul 21;109(28):6147-53. doi: 10.1021/jp051677h. PMID: 16833954.
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Ultrafast charge separation in a photoreactive rhenium-appended porphyrin assembly monitored by picosecond transient infrared spectroscopy.

Journal of the American Chemical Society

Gabrielsson A, Hartl F, Zhang H, Lindsay Smith JR, Towrie M, Vlcek A, Perutz RN.
PMID: 16569000
J Am Chem Soc. 2006 Apr 05;128(13):4253-66. doi: 10.1021/ja0539802.

Rhenium(bipyridine)(tricarbonyl)(picoline) units have been linked covalently to tetraphenylmetalloporphyrins of magnesium and zinc via an amide bond between the bipyridine and one phenyl substituent of the porphyrin. The resulting complexes, abbreviated as [Re(CO)(3)(Pic)Bpy-MgTPP][OTf] and [Re(CO)(3)(Pic)Bpy-ZnTPP][OTf], exhibit no signs of electronic...

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Gabrielsson A, Hartl F, Zhang H, et al. Ultrafast charge separation in a photoreactive rhenium-appended porphyrin assembly monitored by picosecond transient infrared spectroscopy. J Am Chem Soc. 2006;128(13):4253-66doi: 10.1021/ja0539802.
Gabrielsson, A., Hartl, F., Zhang, H., Lindsay Smith, J. R., Towrie, M., Vlcek, A., & Perutz, R. N. (2006). Ultrafast charge separation in a photoreactive rhenium-appended porphyrin assembly monitored by picosecond transient infrared spectroscopy. Journal of the American Chemical Society, 128(13), 4253-66. https://doi.org/10.1021/ja0539802
Gabrielsson, Anders, et al. "Ultrafast charge separation in a photoreactive rhenium-appended porphyrin assembly monitored by picosecond transient infrared spectroscopy." Journal of the American Chemical Society vol. 128,13 (2006): 4253-66. doi: https://doi.org/10.1021/ja0539802
Gabrielsson A, Hartl F, Zhang H, Lindsay Smith JR, Towrie M, Vlcek A, Perutz RN. Ultrafast charge separation in a photoreactive rhenium-appended porphyrin assembly monitored by picosecond transient infrared spectroscopy. J Am Chem Soc. 2006 Apr 05;128(13):4253-66. doi: 10.1021/ja0539802. PMID: 16569000.
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Gene promoter hypermethylation in tumors and plasma of breast cancer patients.

Cancer research and treatment

Bae YK, Shim YR, Choi JH, Kim MJ, Gabrielson E, Lee SJ, Hwang TY, Shin SO.
PMID: 19956520
Cancer Res Treat. 2005 Aug;37(4):233-40. doi: 10.4143/crt.2005.37.4.233. Epub 2005 Aug 31.

PURPOSE: To measure the hypermethylation of four genes in primary tumors and paired plasma samples to determine the feasibility of gene promoter hypermethylation markers for detecting breast cancer in the plasma.MATERIALS AND METHODS: DNA was extracted from the tumor...

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Bae YK, Shim YR, Choi JH, et al. Gene promoter hypermethylation in tumors and plasma of breast cancer patients. Cancer Res Treat. 2005;37(4):233-40doi: 10.4143/crt.2005.37.4.233.
Bae, Y. K., Shim, Y. R., Choi, J. H., Kim, M. J., Gabrielson, E., Lee, S. J., Hwang, T. Y., & Shin, S. O. (2005). Gene promoter hypermethylation in tumors and plasma of breast cancer patients. Cancer research and treatment, 37(4), 233-40. https://doi.org/10.4143/crt.2005.37.4.233
Bae, Young Kyung, et al. "Gene promoter hypermethylation in tumors and plasma of breast cancer patients." Cancer research and treatment vol. 37,4 (2005): 233-40. doi: https://doi.org/10.4143/crt.2005.37.4.233
Bae YK, Shim YR, Choi JH, Kim MJ, Gabrielson E, Lee SJ, Hwang TY, Shin SO. Gene promoter hypermethylation in tumors and plasma of breast cancer patients. Cancer Res Treat. 2005 Aug;37(4):233-40. doi: 10.4143/crt.2005.37.4.233. Epub 2005 Aug 31. PMID: 19956520; PMCID: PMC2785919.
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Comparing spiro-OMeTAD and P3HT hole conductors in efficient solid state dye-sensitized solar cells.

Physical chemistry chemical physics : PCCP

Yang L, Cappel UB, Unger EL, Karlsson M, Karlsson KM, Gabrielsson E, Sun L, Boschloo G, Hagfeldt A, Johansson EM.
PMID: 22116450
Phys Chem Chem Phys. 2012 Jan 14;14(2):779-89. doi: 10.1039/c1cp23031j. Epub 2011 Nov 25.

Two hole conductor materials, spiro-OMeTAD and P3HT, were compared in solid-state dye-sensitized solar cells. Two organic dyes containing one anchor unit (D35) or two anchor units (M3) were used in the comparison. Absorbed photon to current conversion efficiency close...

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Yang L, Cappel UB, Unger EL, et al. Comparing spiro-OMeTAD and P3HT hole conductors in efficient solid state dye-sensitized solar cells. Phys Chem Chem Phys. 2011;14(2):779-89doi: 10.1039/c1cp23031j.
Yang, L., Cappel, U. B., Unger, E. L., Karlsson, M., Karlsson, K. M., Gabrielsson, E., Sun, L., Boschloo, G., Hagfeldt, A., & Johansson, E. M. (2012). Comparing spiro-OMeTAD and P3HT hole conductors in efficient solid state dye-sensitized solar cells. Physical chemistry chemical physics : PCCP, 14(2), 779-89. https://doi.org/10.1039/c1cp23031j
Yang, Lei, et al. "Comparing spiro-OMeTAD and P3HT hole conductors in efficient solid state dye-sensitized solar cells." Physical chemistry chemical physics : PCCP vol. 14,2 (2012): 779-89. doi: https://doi.org/10.1039/c1cp23031j
Yang L, Cappel UB, Unger EL, Karlsson M, Karlsson KM, Gabrielsson E, Sun L, Boschloo G, Hagfeldt A, Johansson EM. Comparing spiro-OMeTAD and P3HT hole conductors in efficient solid state dye-sensitized solar cells. Phys Chem Chem Phys. 2012 Jan 14;14(2):779-89. doi: 10.1039/c1cp23031j. Epub 2011 Nov 25. PMID: 22116450.
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Cancer immunotherapy with exosomes requires B-cell activation.

Oncoimmunology

Näslund TI, Gehrmann U, Gabrielsson S.
PMID: 23894715
Oncoimmunology. 2013 Jun 01;2(6):e24533. doi: 10.4161/onci.24533. Epub 2013 Apr 16.

Exosomes derived from dendritic cells (dexosomes) induce potent antitumor immune responses in mice. We have shown that the efficacy of dexosome-elicited antitumor immunity relies on the presence of both T- and B-cell dexosome-associated epitopes. Hence, the inclusion of B-cell...

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Näslund TI, Gehrmann U, Gabrielsson S. Cancer immunotherapy with exosomes requires B-cell activation. Oncoimmunology. 2013;2(6):e24533doi: 10.4161/onci.24533.
Näslund, T. I., Gehrmann, U., & Gabrielsson, S. (2013). Cancer immunotherapy with exosomes requires B-cell activation. Oncoimmunology, 2(6), e24533. https://doi.org/10.4161/onci.24533
Näslund, Tanja I, et al. "Cancer immunotherapy with exosomes requires B-cell activation." Oncoimmunology vol. 2,6 (2013): e24533. doi: https://doi.org/10.4161/onci.24533
Näslund TI, Gehrmann U, Gabrielsson S. Cancer immunotherapy with exosomes requires B-cell activation. Oncoimmunology. 2013 Jun 01;2(6):e24533. doi: 10.4161/onci.24533. Epub 2013 Apr 16. PMID: 23894715; PMCID: PMC3716750.
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Design of organic dyes and cobalt polypyridine redox mediators for high-efficiency dye-sensitized solar cells.

Journal of the American Chemical Society

Feldt SM, Gibson EA, Gabrielsson E, Sun L, Boschloo G, Hagfeldt A.
PMID: 21047080
J Am Chem Soc. 2010 Nov 24;132(46):16714-24. doi: 10.1021/ja1088869. Epub 2010 Nov 03.

Dye-sensitized solar cells (DSCs) with cobalt-based mediators with efficiencies surpassing the record for DSCs with iodide-free electrolytes were developed by selecting a suitable combination of a cobalt polypyridine complex and an organic sensitizer. The effect of the steric properties...

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Feldt SM, Gibson EA, Gabrielsson E, et al. Design of organic dyes and cobalt polypyridine redox mediators for high-efficiency dye-sensitized solar cells. J Am Chem Soc. 2010;132(46):16714-24doi: 10.1021/ja1088869.
Feldt, S. M., Gibson, E. A., Gabrielsson, E., Sun, L., Boschloo, G., & Hagfeldt, A. (2010). Design of organic dyes and cobalt polypyridine redox mediators for high-efficiency dye-sensitized solar cells. Journal of the American Chemical Society, 132(46), 16714-24. https://doi.org/10.1021/ja1088869
Feldt, Sandra M, et al. "Design of organic dyes and cobalt polypyridine redox mediators for high-efficiency dye-sensitized solar cells." Journal of the American Chemical Society vol. 132,46 (2010): 16714-24. doi: https://doi.org/10.1021/ja1088869
Feldt SM, Gibson EA, Gabrielsson E, Sun L, Boschloo G, Hagfeldt A. Design of organic dyes and cobalt polypyridine redox mediators for high-efficiency dye-sensitized solar cells. J Am Chem Soc. 2010 Nov 24;132(46):16714-24. doi: 10.1021/ja1088869. Epub 2010 Nov 03. PMID: 21047080.
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Showing 1 to 12 of 123 entries