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Spectral and dynamical properties of a Zr-based MOF.

Physical chemistry chemical physics : PCCP

Gutiérrez M, Sánchez F, Douhal A.
PMID: 26400004
Phys Chem Chem Phys. 2016 Feb 21;18(7):5112-20. doi: 10.1039/c5cp04436g. Epub 2015 Sep 24.

We report on the spectra and dynamics of a Zr-naphthalene dicarboxylic acid (Zr-NDC) MOF in different diluted solvent suspensions and in a concentrated tetrahydrofuran (THF) one. In a diluted diethyl ether (DE) suspension, we observed intraparticle excimer formation between...

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Gutiérrez M, Sánchez F, Douhal A. Spectral and dynamical properties of a Zr-based MOF. Phys Chem Chem Phys. 2015;18(7):5112-20doi: 10.1039/c5cp04436g.
Gutiérrez, M., Sánchez, F., & Douhal, A. (2016). Spectral and dynamical properties of a Zr-based MOF. Physical chemistry chemical physics : PCCP, 18(7), 5112-20. https://doi.org/10.1039/c5cp04436g
Gutiérrez, Mario, et al. "Spectral and dynamical properties of a Zr-based MOF." Physical chemistry chemical physics : PCCP vol. 18,7 (2016): 5112-20. doi: https://doi.org/10.1039/c5cp04436g
Gutiérrez M, Sánchez F, Douhal A. Spectral and dynamical properties of a Zr-based MOF. Phys Chem Chem Phys. 2016 Feb 21;18(7):5112-20. doi: 10.1039/c5cp04436g. Epub 2015 Sep 24. PMID: 26400004.
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Toward the design of alkynylimidazole fluorophores: computational and experimental characterization of spectroscopic features in solution and in poly(methyl methacrylate).

Physical chemistry chemical physics : PCCP

Barone V, Bellina F, Biczysko M, Bloino J, Fornaro T, Latouche C, Lessi M, Marianetti G, Minei P, Panattoni A, Pucci A.
PMID: 26395207
Phys Chem Chem Phys. 2015 Oct 28;17(40):26710-23. doi: 10.1039/c5cp03047a.

The possibilities offered by organic fluorophores in the preparation of advanced plastic materials have been increased by designing novel alkynylimidazole dyes, featuring different push and pull groups. This new family of fluorescent dyes was synthesized by means of a...

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Barone V, Bellina F, Biczysko M, et al. Toward the design of alkynylimidazole fluorophores: computational and experimental characterization of spectroscopic features in solution and in poly(methyl methacrylate). Phys Chem Chem Phys. 2015;17(40):26710-23doi: 10.1039/c5cp03047a.
Barone, V., Bellina, F., Biczysko, M., Bloino, J., Fornaro, T., Latouche, C., Lessi, M., Marianetti, G., Minei, P., Panattoni, A., & Pucci, A. (2015). Toward the design of alkynylimidazole fluorophores: computational and experimental characterization of spectroscopic features in solution and in poly(methyl methacrylate). Physical chemistry chemical physics : PCCP, 17(40), 26710-23. https://doi.org/10.1039/c5cp03047a
Barone, Vincenzo, et al. "Toward the design of alkynylimidazole fluorophores: computational and experimental characterization of spectroscopic features in solution and in poly(methyl methacrylate)." Physical chemistry chemical physics : PCCP vol. 17,40 (2015): 26710-23. doi: https://doi.org/10.1039/c5cp03047a
Barone V, Bellina F, Biczysko M, Bloino J, Fornaro T, Latouche C, Lessi M, Marianetti G, Minei P, Panattoni A, Pucci A. Toward the design of alkynylimidazole fluorophores: computational and experimental characterization of spectroscopic features in solution and in poly(methyl methacrylate). Phys Chem Chem Phys. 2015 Oct 28;17(40):26710-23. doi: 10.1039/c5cp03047a. PMID: 26395207; PMCID: PMC5892707.
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Simultaneous spectroscopic measurements of the interior temperature and induced cargo release from pore-restricted mesoporous silica nanoparticles.

Nanoscale

Dong J, Zink JI.
PMID: 27150579
Nanoscale. 2016 May 19;8(20):10558-63. doi: 10.1039/c6nr00978f.

Temperature changes initiated within nano structures are being increasingly used to externally activate responsive delivery vehicles. Yet, the precise measurement of the nano environment temperature increase and its correlation with the induced macroscopic cargo release are difficult to achieve....

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Dong J, Zink JI. Simultaneous spectroscopic measurements of the interior temperature and induced cargo release from pore-restricted mesoporous silica nanoparticles. Nanoscale. 2016;8(20):10558-63doi: 10.1039/c6nr00978f.
Dong, J., & Zink, J. I. (2016). Simultaneous spectroscopic measurements of the interior temperature and induced cargo release from pore-restricted mesoporous silica nanoparticles. Nanoscale, 8(20), 10558-63. https://doi.org/10.1039/c6nr00978f
Dong, Juyao, and Zink, Jeffrey I. "Simultaneous spectroscopic measurements of the interior temperature and induced cargo release from pore-restricted mesoporous silica nanoparticles." Nanoscale vol. 8,20 (2016): 10558-63. doi: https://doi.org/10.1039/c6nr00978f
Dong J, Zink JI. Simultaneous spectroscopic measurements of the interior temperature and induced cargo release from pore-restricted mesoporous silica nanoparticles. Nanoscale. 2016 May 19;8(20):10558-63. doi: 10.1039/c6nr00978f. PMID: 27150579.
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Carbon Nanomembranes.

Advanced materials (Deerfield Beach, Fla.)

Turchanin A, Gölzhäuser A.
PMID: 27281234
Adv Mater. 2016 Aug;28(29):6075-103. doi: 10.1002/adma.201506058. Epub 2016 Jun 09.

Carbon nanomembranes (CNMs) are synthetic 2D carbon sheets with tailored physical or chemical properties. These depend on the structure, molecular composition, and surroundings on either side. Due to their molecular thickness, they can be regarded as "interfaces without bulk"...

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Turchanin A, Gölzhäuser A. Carbon Nanomembranes. Adv Mater. 2016;28(29):6075-103doi: 10.1002/adma.201506058.
Turchanin, A., & Gölzhäuser, A. (2016). Carbon Nanomembranes. Advanced materials (Deerfield Beach, Fla.), 28(29), 6075-103. https://doi.org/10.1002/adma.201506058
Turchanin, Andrey, and Gölzhäuser, Armin. "Carbon Nanomembranes." Advanced materials (Deerfield Beach, Fla.) vol. 28,29 (2016): 6075-103. doi: https://doi.org/10.1002/adma.201506058
Turchanin A, Gölzhäuser A. Carbon Nanomembranes. Adv Mater. 2016 Aug;28(29):6075-103. doi: 10.1002/adma.201506058. Epub 2016 Jun 09. PMID: 27281234.
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Induction of Strong and Tunable Circularly Polarized Luminescence of Nonchiral, Nonmetal, Low-Molecular-Weight Fluorophores Using Chiral Nanotemplates.

Angewandte Chemie (International ed. in English)

Goto T, Okazaki Y, Ueki M, Kuwahara Y, Takafuji M, Oda R, Ihara H.
PMID: 28146313
Angew Chem Int Ed Engl. 2017 Mar 06;56(11):2989-2993. doi: 10.1002/anie.201612331. Epub 2017 Jan 31.

A new strategy is described for generating strong circularly polarized luminescence with highly tunable emission bands through chiral induction in nonchiral, totally organic, low-molecular-weight fluorescent dyes by chiral nanotemplate systems. Our approach allows the first systematic investigation to clarify...

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Goto T, Okazaki Y, Ueki M, et al. Induction of Strong and Tunable Circularly Polarized Luminescence of Nonchiral, Nonmetal, Low-Molecular-Weight Fluorophores Using Chiral Nanotemplates. Angew Chem Int Ed Engl. 2017;56(11):2989-2993doi: 10.1002/anie.201612331.
Goto, T., Okazaki, Y., Ueki, M., Kuwahara, Y., Takafuji, M., Oda, R., & Ihara, H. (2017). Induction of Strong and Tunable Circularly Polarized Luminescence of Nonchiral, Nonmetal, Low-Molecular-Weight Fluorophores Using Chiral Nanotemplates. Angewandte Chemie (International ed. in English), 56(11), 2989-2993. https://doi.org/10.1002/anie.201612331
Goto, Taisei, et al. "Induction of Strong and Tunable Circularly Polarized Luminescence of Nonchiral, Nonmetal, Low-Molecular-Weight Fluorophores Using Chiral Nanotemplates." Angewandte Chemie (International ed. in English) vol. 56,11 (2017): 2989-2993. doi: https://doi.org/10.1002/anie.201612331
Goto T, Okazaki Y, Ueki M, Kuwahara Y, Takafuji M, Oda R, Ihara H. Induction of Strong and Tunable Circularly Polarized Luminescence of Nonchiral, Nonmetal, Low-Molecular-Weight Fluorophores Using Chiral Nanotemplates. Angew Chem Int Ed Engl. 2017 Mar 06;56(11):2989-2993. doi: 10.1002/anie.201612331. Epub 2017 Jan 31. PMID: 28146313.
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Curcuminoid-BF.

Beilstein journal of organic chemistry

Weiss H, Reichel J, Görls H, Schneider KRA, Micheel M, Pröhl M, Gottschaldt M, Dietzek B, Weigand W.
PMID: 29114330
Beilstein J Org Chem. 2017 Oct 26;13:2264-2272. doi: 10.3762/bjoc.13.223. eCollection 2017.

Eight difluoroboron complexes of curcumin derivatives carrying alkyne groups containing substituents have been synthesized following an optimised reaction pathway. The complexes were received in yields up to 98% and high purities. Their properties as fluorescent dyes have been investigated....

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Weiss H, Reichel J, Görls H, et al. Curcuminoid-BF. Beilstein J Org Chem. 2017;13:2264-2272doi: 10.3762/bjoc.13.223.
Weiss, H., Reichel, J., Görls, H., Schneider, K. R. A., Micheel, M., Pröhl, M., Gottschaldt, M., Dietzek, B., & Weigand, W. (2017). Curcuminoid-BF. Beilstein journal of organic chemistry, 132264-2272. https://doi.org/10.3762/bjoc.13.223
Weiss, Henning, et al. "Curcuminoid-BF." Beilstein journal of organic chemistry vol. 13 (2017): 2264-2272. doi: https://doi.org/10.3762/bjoc.13.223
Weiss H, Reichel J, Görls H, Schneider KRA, Micheel M, Pröhl M, Gottschaldt M, Dietzek B, Weigand W. Curcuminoid-BF. Beilstein J Org Chem. 2017 Oct 26;13:2264-2272. doi: 10.3762/bjoc.13.223. eCollection 2017. PMID: 29114330; PMCID: PMC5669223.
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Bright Fluorescent Nanotags from Bottlebrush Polymers with DNA-Tipped Bristles.

ACS central science

Fouz MF, Mukumoto K, Averick S, Molinar O, McCartney BM, Matyjaszewski K, Armitage BA, Das SR.
PMID: 27163005
ACS Cent Sci. 2015 Nov 25;1(8):431-8. doi: 10.1021/acscentsci.5b00259. Epub 2015 Nov 04.

Bright signal outputs are needed for fluorescence detection of biomolecules at their native expression levels. Increasing the number of labels on a probe often results in crowding-induced self-quenching of chromophores, and maintaining the function of the targeting moiety (e.g.,...

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Fouz MF, Mukumoto K, Averick S, et al. Bright Fluorescent Nanotags from Bottlebrush Polymers with DNA-Tipped Bristles. ACS Cent Sci. 2015;1(8):431-8doi: 10.1021/acscentsci.5b00259.
Fouz, M. F., Mukumoto, K., Averick, S., Molinar, O., McCartney, B. M., Matyjaszewski, K., Armitage, B. A., & Das, S. R. (2015). Bright Fluorescent Nanotags from Bottlebrush Polymers with DNA-Tipped Bristles. ACS central science, 1(8), 431-8. https://doi.org/10.1021/acscentsci.5b00259
Fouz, Munira F, et al. "Bright Fluorescent Nanotags from Bottlebrush Polymers with DNA-Tipped Bristles." ACS central science vol. 1,8 (2015): 431-8. doi: https://doi.org/10.1021/acscentsci.5b00259
Fouz MF, Mukumoto K, Averick S, Molinar O, McCartney BM, Matyjaszewski K, Armitage BA, Das SR. Bright Fluorescent Nanotags from Bottlebrush Polymers with DNA-Tipped Bristles. ACS Cent Sci. 2015 Nov 25;1(8):431-8. doi: 10.1021/acscentsci.5b00259. Epub 2015 Nov 04. PMID: 27163005; PMCID: PMC4827471.
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Handheld confocal laser endomicroscopic imaging utilizing tumor-specific fluorescent labeling to identify experimental glioma cells .

Surgical neurology international

Martirosyan NL, Georges J, Kalani MY, Nakaji P, Spetzler RF, Feuerstein BG, Preul MC.
PMID: 28144472
Surg Neurol Int. 2016 Dec 12;7:S995-S1003. doi: 10.4103/2152-7806.195577. eCollection 2016.

BACKGROUND: We have reported that handheld confocal laser endomicroscopy (CLE) can be used with various nonspecific fluorescent dyes to improve the microscopic identification of brain tumor and its boundaries. Here, we show that CLE can be used experimentally with...

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Martirosyan NL, Georges J, Kalani MY, et al. Handheld confocal laser endomicroscopic imaging utilizing tumor-specific fluorescent labeling to identify experimental glioma cells . Surg Neurol Int. 2016;7:S995-S1003doi: 10.4103/2152-7806.195577.
Martirosyan, N. L., Georges, J., Kalani, M. Y., Nakaji, P., Spetzler, R. F., Feuerstein, B. G., & Preul, M. C. (2016). Handheld confocal laser endomicroscopic imaging utilizing tumor-specific fluorescent labeling to identify experimental glioma cells . Surgical neurology international, 7S995-S1003. https://doi.org/10.4103/2152-7806.195577
Martirosyan, Nikolay L, et al. "Handheld confocal laser endomicroscopic imaging utilizing tumor-specific fluorescent labeling to identify experimental glioma cells ." Surgical neurology international vol. 7 (2016): S995-S1003. doi: https://doi.org/10.4103/2152-7806.195577
Martirosyan NL, Georges J, Kalani MY, Nakaji P, Spetzler RF, Feuerstein BG, Preul MC. Handheld confocal laser endomicroscopic imaging utilizing tumor-specific fluorescent labeling to identify experimental glioma cells . Surg Neurol Int. 2016 Dec 12;7:S995-S1003. doi: 10.4103/2152-7806.195577. eCollection 2016. PMID: 28144472; PMCID: PMC5234279.
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The fluorescent pentameric oligothiophene pFTAA identifies filamentous tau in live neurons cultured from adult P301S tau mice.

Frontiers in neuroscience

Brelstaff J, Ossola B, Neher JJ, Klingstedt T, Nilsson KP, Goedert M, Spillantini MG, Tolkovsky AM.
PMID: 26074756
Front Neurosci. 2015 May 29;9:184. doi: 10.3389/fnins.2015.00184. eCollection 2015.

Identification of fluorescent dyes that label the filamentous protein aggregates characteristic of neurodegenerative disease, such as β-amyloid and tau in Alzheimer's disease, in a live cell culture system has previously been a major hurdle. Here we show that pentameric...

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Brelstaff J, Ossola B, Neher JJ, et al. The fluorescent pentameric oligothiophene pFTAA identifies filamentous tau in live neurons cultured from adult P301S tau mice. Front Neurosci. 2015;9:184doi: 10.3389/fnins.2015.00184.
Brelstaff, J., Ossola, B., Neher, J. J., Klingstedt, T., Nilsson, K. P., Goedert, M., Spillantini, M. G., & Tolkovsky, A. M. (2015). The fluorescent pentameric oligothiophene pFTAA identifies filamentous tau in live neurons cultured from adult P301S tau mice. Frontiers in neuroscience, 9184. https://doi.org/10.3389/fnins.2015.00184
Brelstaff, Jack, et al. "The fluorescent pentameric oligothiophene pFTAA identifies filamentous tau in live neurons cultured from adult P301S tau mice." Frontiers in neuroscience vol. 9 (2015): 184. doi: https://doi.org/10.3389/fnins.2015.00184
Brelstaff J, Ossola B, Neher JJ, Klingstedt T, Nilsson KP, Goedert M, Spillantini MG, Tolkovsky AM. The fluorescent pentameric oligothiophene pFTAA identifies filamentous tau in live neurons cultured from adult P301S tau mice. Front Neurosci. 2015 May 29;9:184. doi: 10.3389/fnins.2015.00184. eCollection 2015. PMID: 26074756; PMCID: PMC4448042.
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Inclusion of push-pull N-methylpyridinium salts within surfactant hydrogels: is their excited state intramolecular charge transfer mediated by twisting?.

Physical chemistry chemical physics : PCCP

Cesaretti A, Carlotti B, Germani R, Spalletti A, Elisei F.
PMID: 26073742
Phys Chem Chem Phys. 2015 Jul 14;17(26):17214-20. doi: 10.1039/c5cp01639h.

In order to get a deep insight into the environment-dependent photophysics of push-pull pyridinium derivatives, two N-methylpyridinium salts were dissolved within surfactant hydrogels. Surfactant viscoelastic solutions can potentially block or at least limit the torsion of these fluorescent dyes,...

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Cesaretti A, Carlotti B, Germani R, et al. Inclusion of push-pull N-methylpyridinium salts within surfactant hydrogels: is their excited state intramolecular charge transfer mediated by twisting?. Phys Chem Chem Phys. 2015;17(26):17214-20doi: 10.1039/c5cp01639h.
Cesaretti, A., Carlotti, B., Germani, R., Spalletti, A., & Elisei, F. (2015). Inclusion of push-pull N-methylpyridinium salts within surfactant hydrogels: is their excited state intramolecular charge transfer mediated by twisting?. Physical chemistry chemical physics : PCCP, 17(26), 17214-20. https://doi.org/10.1039/c5cp01639h
Cesaretti, A, et al. "Inclusion of push-pull N-methylpyridinium salts within surfactant hydrogels: is their excited state intramolecular charge transfer mediated by twisting?." Physical chemistry chemical physics : PCCP vol. 17,26 (2015): 17214-20. doi: https://doi.org/10.1039/c5cp01639h
Cesaretti A, Carlotti B, Germani R, Spalletti A, Elisei F. Inclusion of push-pull N-methylpyridinium salts within surfactant hydrogels: is their excited state intramolecular charge transfer mediated by twisting?. Phys Chem Chem Phys. 2015 Jul 14;17(26):17214-20. doi: 10.1039/c5cp01639h. PMID: 26073742.
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Synthesis and Fluorescence Properties of Pyrimidine-Based Diboron Complexes with Donor-π-Acceptor Structures.

Chemistry (Weinheim an der Bergstrasse, Germany)

Kubota Y, Kasatani K, Niwa T, Sato H, Funabiki K, Matsui M.
PMID: 26670268
Chemistry. 2016 Jan 26;22(5):1816-24. doi: 10.1002/chem.201503625. Epub 2015 Dec 16.

Pyrimidine-based diboron complexes bearing β-iminoenolate ligands and phenyl groups as bulky substituents on the boron atoms were synthesized as novel fluorescent dyes, and their fluorescence properties were investigated in solution and in the solid state. The diboron complexes with...

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Kubota Y, Kasatani K, Niwa T, et al. Synthesis and Fluorescence Properties of Pyrimidine-Based Diboron Complexes with Donor-π-Acceptor Structures. Chemistry. 2015;22(5):1816-24doi: 10.1002/chem.201503625.
Kubota, Y., Kasatani, K., Niwa, T., Sato, H., Funabiki, K., & Matsui, M. (2016). Synthesis and Fluorescence Properties of Pyrimidine-Based Diboron Complexes with Donor-π-Acceptor Structures. Chemistry (Weinheim an der Bergstrasse, Germany), 22(5), 1816-24. https://doi.org/10.1002/chem.201503625
Kubota, Yasuhiro, et al. "Synthesis and Fluorescence Properties of Pyrimidine-Based Diboron Complexes with Donor-π-Acceptor Structures." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 22,5 (2016): 1816-24. doi: https://doi.org/10.1002/chem.201503625
Kubota Y, Kasatani K, Niwa T, Sato H, Funabiki K, Matsui M. Synthesis and Fluorescence Properties of Pyrimidine-Based Diboron Complexes with Donor-π-Acceptor Structures. Chemistry. 2016 Jan 26;22(5):1816-24. doi: 10.1002/chem.201503625. Epub 2015 Dec 16. PMID: 26670268.
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Concentrating aggregation-induced fluorescence in planar waveguides: a proof-of-principle.

Scientific reports

Banal JL, White JM, Ghiggino KP, Wong WW.
PMID: 24844675
Sci Rep. 2014 Apr 10;4:4635. doi: 10.1038/srep04635.

The photophysical properties of fluorescent dyes are key determinants in the performance of luminescent solar concentrators (LSCs). First-generation dyes--coumarin, perylenes, and rhodamines--used in LSCs suffer from both concentration quenching in the solid-state and small Stokes shifts which limit the...

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Banal JL, White JM, Ghiggino KP, et al. Concentrating aggregation-induced fluorescence in planar waveguides: a proof-of-principle. Sci Rep. 2014;4:4635doi: 10.1038/srep04635.
Banal, J. L., White, J. M., Ghiggino, K. P., & Wong, W. W. (2014). Concentrating aggregation-induced fluorescence in planar waveguides: a proof-of-principle. Scientific reports, 44635. https://doi.org/10.1038/srep04635
Banal, James L, et al. "Concentrating aggregation-induced fluorescence in planar waveguides: a proof-of-principle." Scientific reports vol. 4 (2014): 4635. doi: https://doi.org/10.1038/srep04635
Banal JL, White JM, Ghiggino KP, Wong WW. Concentrating aggregation-induced fluorescence in planar waveguides: a proof-of-principle. Sci Rep. 2014 Apr 10;4:4635. doi: 10.1038/srep04635. PMID: 24844675; PMCID: PMC4027885.
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Showing 1 to 12 of 987 entries