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Two-Dimensional Topological Insulators: Progress and Prospects.

The journal of physical chemistry letters

Kou L, Ma Y, Sun Z, Heine T, Chen C.
PMID: 28394616
J Phys Chem Lett. 2017 Apr 20;8(8):1905-1919. doi: 10.1021/acs.jpclett.7b00222. Epub 2017 Apr 14.

Two-dimensional topological insulators (2D TIs) are a remarkable class of atomically thin layered materials that exhibit unique symmetry-protected helical metallic edge states with an insulating interior. Recent years have seen a tremendous surge in research of this intriguing new...

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Kou L, Ma Y, Sun Z, et al. Two-Dimensional Topological Insulators: Progress and Prospects. J Phys Chem Lett. 2017;8(8):1905-1919doi: 10.1021/acs.jpclett.7b00222.
Kou, L., Ma, Y., Sun, Z., Heine, T., & Chen, C. (2017). Two-Dimensional Topological Insulators: Progress and Prospects. The journal of physical chemistry letters, 8(8), 1905-1919. https://doi.org/10.1021/acs.jpclett.7b00222
Kou, Liangzhi, et al. "Two-Dimensional Topological Insulators: Progress and Prospects." The journal of physical chemistry letters vol. 8,8 (2017): 1905-1919. doi: https://doi.org/10.1021/acs.jpclett.7b00222
Kou L, Ma Y, Sun Z, Heine T, Chen C. Two-Dimensional Topological Insulators: Progress and Prospects. J Phys Chem Lett. 2017 Apr 20;8(8):1905-1919. doi: 10.1021/acs.jpclett.7b00222. Epub 2017 Apr 14. PMID: 28394616.
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A photorespiratory bypass increases plant growth and seed yield in biofuel crop Camelina sativa.

Biotechnology for biofuels

Dalal J, Lopez H, Vasani NB, Hu Z, Swift JE, Yalamanchili R, Dvora M, Lin X, Xie D, Qu R, Sederoff HW.
PMID: 26516348
Biotechnol Biofuels. 2015 Oct 29;8:175. doi: 10.1186/s13068-015-0357-1. eCollection 2015.

BACKGROUND: Camelina sativa is an oilseed crop with great potential for biofuel production on marginal land. The seed oil from camelina has been converted to jet fuel and improved fuel efficiency in commercial and military test flights. Hydrogenation-derived renewable...

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Dalal J, Lopez H, Vasani NB, et al. A photorespiratory bypass increases plant growth and seed yield in biofuel crop Camelina sativa. Biotechnol Biofuels. 2015;8:175doi: 10.1186/s13068-015-0357-1.
Dalal, J., Lopez, H., Vasani, N. B., Hu, Z., Swift, J. E., Yalamanchili, R., Dvora, M., Lin, X., Xie, D., Qu, R., & Sederoff, H. W. (2015). A photorespiratory bypass increases plant growth and seed yield in biofuel crop Camelina sativa. Biotechnology for biofuels, 8175. https://doi.org/10.1186/s13068-015-0357-1
Dalal, Jyoti, et al. "A photorespiratory bypass increases plant growth and seed yield in biofuel crop Camelina sativa." Biotechnology for biofuels vol. 8 (2015): 175. doi: https://doi.org/10.1186/s13068-015-0357-1
Dalal J, Lopez H, Vasani NB, Hu Z, Swift JE, Yalamanchili R, Dvora M, Lin X, Xie D, Qu R, Sederoff HW. A photorespiratory bypass increases plant growth and seed yield in biofuel crop Camelina sativa. Biotechnol Biofuels. 2015 Oct 29;8:175. doi: 10.1186/s13068-015-0357-1. eCollection 2015. PMID: 26516348; PMCID: PMC4625952.
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Modeling CO2 reduction on Pt(111).

Physical chemistry chemical physics : PCCP

Shi C, O'Grady CP, Peterson AA, Hansen HA, Nørskov JK.
PMID: 23552398
Phys Chem Chem Phys. 2013 May 21;15(19):7114-22. doi: 10.1039/c3cp50645b.

Density functional theory was used to model the electrochemical reduction of CO2 on Pt(111) with an explicit solvation layer and the presence of extra hydrogen atoms to represent a negatively charged electrode. We focused on the electronic energy barriers...

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Shi C, O'Grady CP, Peterson AA, et al. Modeling CO2 reduction on Pt(111). Phys Chem Chem Phys. 2013;15(19):7114-22doi: 10.1039/c3cp50645b.
Shi, C., O'Grady, C. P., Peterson, A. A., Hansen, H. A., & Nørskov, J. K. (2013). Modeling CO2 reduction on Pt(111). Physical chemistry chemical physics : PCCP, 15(19), 7114-22. https://doi.org/10.1039/c3cp50645b
Shi, Chuan, et al. "Modeling CO2 reduction on Pt(111)." Physical chemistry chemical physics : PCCP vol. 15,19 (2013): 7114-22. doi: https://doi.org/10.1039/c3cp50645b
Shi C, O'Grady CP, Peterson AA, Hansen HA, Nørskov JK. Modeling CO2 reduction on Pt(111). Phys Chem Chem Phys. 2013 May 21;15(19):7114-22. doi: 10.1039/c3cp50645b. PMID: 23552398.
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Enhancement of chemical stability and crystallinity in porphyrin-containing covalent organic frameworks by intramolecular hydrogen bonds.

Angewandte Chemie (International ed. in English)

Kandambeth S, Shinde DB, Panda MK, Lukose B, Heine T, Banerjee R.
PMID: 24127339
Angew Chem Int Ed Engl. 2013 Dec 02;52(49):13052-6. doi: 10.1002/anie.201306775. Epub 2013 Oct 14.

A strong bond: A strategy based on intramolecular hydrogen-binding interactions in 2D covalent organic frameworks (COFs) is shown to improve the crystallinity, porosity, and chemical stability of the material. The concept is validated by removing the hydrogen-bonding interaction in...

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Kandambeth S, Shinde DB, Panda MK, et al. Enhancement of chemical stability and crystallinity in porphyrin-containing covalent organic frameworks by intramolecular hydrogen bonds. Angew Chem Int Ed Engl. 2013;52(49):13052-6doi: 10.1002/anie.201306775.
Kandambeth, S., Shinde, D. B., Panda, M. K., Lukose, B., Heine, T., & Banerjee, R. (2013). Enhancement of chemical stability and crystallinity in porphyrin-containing covalent organic frameworks by intramolecular hydrogen bonds. Angewandte Chemie (International ed. in English), 52(49), 13052-6. https://doi.org/10.1002/anie.201306775
Kandambeth, Sharath, et al. "Enhancement of chemical stability and crystallinity in porphyrin-containing covalent organic frameworks by intramolecular hydrogen bonds." Angewandte Chemie (International ed. in English) vol. 52,49 (2013): 13052-6. doi: https://doi.org/10.1002/anie.201306775
Kandambeth S, Shinde DB, Panda MK, Lukose B, Heine T, Banerjee R. Enhancement of chemical stability and crystallinity in porphyrin-containing covalent organic frameworks by intramolecular hydrogen bonds. Angew Chem Int Ed Engl. 2013 Dec 02;52(49):13052-6. doi: 10.1002/anie.201306775. Epub 2013 Oct 14. PMID: 24127339.
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Colloidal synthesis of single-layer MSe2 (M = Mo, W) nanosheets via anisotropic solution-phase growth approach.

Journal of the American Chemical Society

Jung W, Lee S, Yoo D, Jeong S, Miró P, Kuc A, Heine T, Cheon J.
PMID: 26053408
J Am Chem Soc. 2015 Jun 17;137(23):7266-9. doi: 10.1021/jacs.5b02772. Epub 2015 Jun 08.

The generation of single-layer 2-dimensional (2D) nanosheets has been challenging, especially in solution-phase, since it requires highly anisotropic growth processes that exclusively promote planar directionality during nanocrystal formation. In this study, we discovered that such selective growth pathways can...

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Jung W, Lee S, Yoo D, et al. Colloidal synthesis of single-layer MSe2 (M = Mo, W) nanosheets via anisotropic solution-phase growth approach. J Am Chem Soc. 2015;137(23):7266-9doi: 10.1021/jacs.5b02772.
Jung, W., Lee, S., Yoo, D., Jeong, S., Miró, P., Kuc, A., Heine, T., & Cheon, J. (2015). Colloidal synthesis of single-layer MSe2 (M = Mo, W) nanosheets via anisotropic solution-phase growth approach. Journal of the American Chemical Society, 137(23), 7266-9. https://doi.org/10.1021/jacs.5b02772
Jung, Wonil, et al. "Colloidal synthesis of single-layer MSe2 (M = Mo, W) nanosheets via anisotropic solution-phase growth approach." Journal of the American Chemical Society vol. 137,23 (2015): 7266-9. doi: https://doi.org/10.1021/jacs.5b02772
Jung W, Lee S, Yoo D, Jeong S, Miró P, Kuc A, Heine T, Cheon J. Colloidal synthesis of single-layer MSe2 (M = Mo, W) nanosheets via anisotropic solution-phase growth approach. J Am Chem Soc. 2015 Jun 17;137(23):7266-9. doi: 10.1021/jacs.5b02772. Epub 2015 Jun 08. PMID: 26053408.
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Exploration of Functional Connectivity During Preferred Music Stimulation in Patients with Disorders of Consciousness.

Frontiers in psychology

Heine L, Castro M, Martial C, Tillmann B, Laureys S, Perrin F.
PMID: 26617542
Front Psychol. 2015 Nov 09;6:1704. doi: 10.3389/fpsyg.2015.01704. eCollection 2015.

Preferred music is a highly emotional and salient stimulus, which has previously been shown to increase the probability of auditory cognitive event-related responses in patients with disorders of consciousness (DOC). To further investigate whether and how music modifies the...

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Heine L, Castro M, Martial C, et al. Exploration of Functional Connectivity During Preferred Music Stimulation in Patients with Disorders of Consciousness. Front Psychol. 2015;6:1704doi: 10.3389/fpsyg.2015.01704.
Heine, L., Castro, M., Martial, C., Tillmann, B., Laureys, S., & Perrin, F. (2015). Exploration of Functional Connectivity During Preferred Music Stimulation in Patients with Disorders of Consciousness. Frontiers in psychology, 61704. https://doi.org/10.3389/fpsyg.2015.01704
Heine, Lizette, et al. "Exploration of Functional Connectivity During Preferred Music Stimulation in Patients with Disorders of Consciousness." Frontiers in psychology vol. 6 (2015): 1704. doi: https://doi.org/10.3389/fpsyg.2015.01704
Heine L, Castro M, Martial C, Tillmann B, Laureys S, Perrin F. Exploration of Functional Connectivity During Preferred Music Stimulation in Patients with Disorders of Consciousness. Front Psychol. 2015 Nov 09;6:1704. doi: 10.3389/fpsyg.2015.01704. eCollection 2015. PMID: 26617542; PMCID: PMC4637404.
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Spectra Transfer Between a Fourier Transform Near-Infrared Laboratory and a Miniaturized Handheld Near-Infrared Spectrometer.

Applied spectroscopy

Hoffmann U, Pfeifer F, Hsuing C, Siesler HW.
PMID: 27170780
Appl Spectrosc. 2016 May;70(5):852-60. doi: 10.1177/0003702816638284.

The aim of this contribution is to demonstrate the transfer of spectra that have been measured on two different laboratory Fourier transform near-infrared (FT-NIR) spectrometers to the format of a handheld instrument by measuring only a few samples with...

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Hoffmann U, Pfeifer F, Hsuing C, et al. Spectra Transfer Between a Fourier Transform Near-Infrared Laboratory and a Miniaturized Handheld Near-Infrared Spectrometer. Appl Spectrosc. 2016;70(5):852-60doi: 10.1177/0003702816638284.
Hoffmann, U., Pfeifer, F., Hsuing, C., & Siesler, H. W. (2016). Spectra Transfer Between a Fourier Transform Near-Infrared Laboratory and a Miniaturized Handheld Near-Infrared Spectrometer. Applied spectroscopy, 70(5), 852-60. https://doi.org/10.1177/0003702816638284
Hoffmann, Uwe, et al. "Spectra Transfer Between a Fourier Transform Near-Infrared Laboratory and a Miniaturized Handheld Near-Infrared Spectrometer." Applied spectroscopy vol. 70,5 (2016): 852-60. doi: https://doi.org/10.1177/0003702816638284
Hoffmann U, Pfeifer F, Hsuing C, Siesler HW. Spectra Transfer Between a Fourier Transform Near-Infrared Laboratory and a Miniaturized Handheld Near-Infrared Spectrometer. Appl Spectrosc. 2016 May;70(5):852-60. doi: 10.1177/0003702816638284. PMID: 27170780.
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Catalytic and hydrodynamic properties of styrene monooxygenases from Rhodococcus opacus 1CP are modulated by cofactor binding.

AMB Express

Riedel A, Heine T, Westphal AH, Conrad C, Rathsack P, van Berkel WJ, Tischler D.
PMID: 26054733
AMB Express. 2015 Dec;5(1):112. doi: 10.1186/s13568-015-0112-9. Epub 2015 Jun 04.

Styrene monooxygenases (SMOs) are flavoenzymes catalyzing the epoxidation of styrene into styrene oxide. SMOs are composed of a monooxygenase (StyA) and a reductase (StyB). The latter delivers reduced FAD to StyA on the expense of NADH. We identified Rhodococcus...

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Riedel A, Heine T, Westphal AH, et al. Catalytic and hydrodynamic properties of styrene monooxygenases from Rhodococcus opacus 1CP are modulated by cofactor binding. AMB Express. 2015;5(1):112doi: 10.1186/s13568-015-0112-9.
Riedel, A., Heine, T., Westphal, A. H., Conrad, C., Rathsack, P., van Berkel, W. J., & Tischler, D. (2015). Catalytic and hydrodynamic properties of styrene monooxygenases from Rhodococcus opacus 1CP are modulated by cofactor binding. AMB Express, 5(1), 112. https://doi.org/10.1186/s13568-015-0112-9
Riedel, Anika, et al. "Catalytic and hydrodynamic properties of styrene monooxygenases from Rhodococcus opacus 1CP are modulated by cofactor binding." AMB Express vol. 5,1 (2015): 112. doi: https://doi.org/10.1186/s13568-015-0112-9
Riedel A, Heine T, Westphal AH, Conrad C, Rathsack P, van Berkel WJ, Tischler D. Catalytic and hydrodynamic properties of styrene monooxygenases from Rhodococcus opacus 1CP are modulated by cofactor binding. AMB Express. 2015 Dec;5(1):112. doi: 10.1186/s13568-015-0112-9. Epub 2015 Jun 04. PMID: 26054733; PMCID: PMC4460183.
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Decoding the Morphological Diversity in Two Dimensional Crystalline Porous Polymers by Core Planarity Modulation.

Angewandte Chemie (International ed. in English)

Halder A, Kandambeth S, Biswal BP, Kaur G, Roy NC, Addicoat M, Salunke JK, Banerjee S, Vanka K, Heine T, Verma S, Banerjee R.
PMID: 26953562
Angew Chem Int Ed Engl. 2016 Jun 27;55(27):7806-10. doi: 10.1002/anie.201600087. Epub 2016 Mar 08.

Two new chemically stable triazine- and phenyl-core-based crystalline porous polymers (CPPs) have been synthesized using a single-step template-free solvothermal route. Unique morphological diversities were observed for these CPPs [2,3-DhaTta (ribbon) and 2,3-DhaTab (hollow sphere)] by simply altering the linker...

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Halder A, Kandambeth S, Biswal BP, et al. Decoding the Morphological Diversity in Two Dimensional Crystalline Porous Polymers by Core Planarity Modulation. Angew Chem Int Ed Engl. 2016;55(27):7806-10doi: 10.1002/anie.201600087.
Halder, A., Kandambeth, S., Biswal, B. P., Kaur, G., Roy, N. C., Addicoat, M., Salunke, J. K., Banerjee, S., Vanka, K., Heine, T., Verma, S., & Banerjee, R. (2016). Decoding the Morphological Diversity in Two Dimensional Crystalline Porous Polymers by Core Planarity Modulation. Angewandte Chemie (International ed. in English), 55(27), 7806-10. https://doi.org/10.1002/anie.201600087
Halder, Arjun, et al. "Decoding the Morphological Diversity in Two Dimensional Crystalline Porous Polymers by Core Planarity Modulation." Angewandte Chemie (International ed. in English) vol. 55,27 (2016): 7806-10. doi: https://doi.org/10.1002/anie.201600087
Halder A, Kandambeth S, Biswal BP, Kaur G, Roy NC, Addicoat M, Salunke JK, Banerjee S, Vanka K, Heine T, Verma S, Banerjee R. Decoding the Morphological Diversity in Two Dimensional Crystalline Porous Polymers by Core Planarity Modulation. Angew Chem Int Ed Engl. 2016 Jun 27;55(27):7806-10. doi: 10.1002/anie.201600087. Epub 2016 Mar 08. PMID: 26953562.
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Temperature Changes in the Altai Are Driven by Solar and Anthropogenic Forcing.

Chimia

Eichler A, Olivier S, Henderson K, Laube A, Beer J, Gäggeler HW, Papina T, Schwikowski M.
PMID: 28372622
Chimia (Aarau). 2009 Dec 01;63(12):889. doi: 10.2533/chimia.2009.889.

No abstract available.

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Eichler A, Olivier S, Henderson K, et al. Temperature Changes in the Altai Are Driven by Solar and Anthropogenic Forcing. Chimia (Aarau). 2009;63(12):889doi: 10.2533/chimia.2009.889.
Eichler, A., Olivier, S., Henderson, K., Laube, A., Beer, J., Gäggeler, H. W., Papina, T., & Schwikowski, M. (2009). Temperature Changes in the Altai Are Driven by Solar and Anthropogenic Forcing. Chimia, 63(12), 889. https://doi.org/10.2533/chimia.2009.889
Eichler, Anja, et al. "Temperature Changes in the Altai Are Driven by Solar and Anthropogenic Forcing." Chimia vol. 63,12 (2009): 889. doi: https://doi.org/10.2533/chimia.2009.889
Eichler A, Olivier S, Henderson K, Laube A, Beer J, Gäggeler HW, Papina T, Schwikowski M. Temperature Changes in the Altai Are Driven by Solar and Anthropogenic Forcing. Chimia (Aarau). 2009 Dec 01;63(12):889. doi: 10.2533/chimia.2009.889. PMID: 28372622.
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Mechanochemical Synthesis of 3d Transition-Metal-1,2,4-Triazole Complexes as Precursors for Microwave-Assisted and Thermal Conversion to Coordination Polymers with a High Influence on the Dielectric Properties.

Chemistry (Weinheim an der Bergstrasse, Germany)

Brede FA, Heine J, Sextl G, Müller-Buschbaum K.
PMID: 26797710
Chemistry. 2016 Feb 18;22(8):2708-18. doi: 10.1002/chem.201503725. Epub 2016 Jan 21.

The complexes [MCl2 (TzH)4] (M=Mn (1), Fe (2); TzH=1,2,4-1H-triazole) and [ZnCl2 (TzH)2] (3) have been obtained by mechanochemical reactions of the corresponding divalent metal chloride and 1,2,4-1H-triazole. They were successfully used as precursors for the formation of coordination polymers...

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Brede FA, Heine J, Sextl G, et al. Mechanochemical Synthesis of 3d Transition-Metal-1,2,4-Triazole Complexes as Precursors for Microwave-Assisted and Thermal Conversion to Coordination Polymers with a High Influence on the Dielectric Properties. Chemistry. 2016;22(8):2708-18doi: 10.1002/chem.201503725.
Brede, F. A., Heine, J., Sextl, G., & Müller-Buschbaum, K. (2016). Mechanochemical Synthesis of 3d Transition-Metal-1,2,4-Triazole Complexes as Precursors for Microwave-Assisted and Thermal Conversion to Coordination Polymers with a High Influence on the Dielectric Properties. Chemistry (Weinheim an der Bergstrasse, Germany), 22(8), 2708-18. https://doi.org/10.1002/chem.201503725
Brede, Franziska A, et al. "Mechanochemical Synthesis of 3d Transition-Metal-1,2,4-Triazole Complexes as Precursors for Microwave-Assisted and Thermal Conversion to Coordination Polymers with a High Influence on the Dielectric Properties." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 22,8 (2016): 2708-18. doi: https://doi.org/10.1002/chem.201503725
Brede FA, Heine J, Sextl G, Müller-Buschbaum K. Mechanochemical Synthesis of 3d Transition-Metal-1,2,4-Triazole Complexes as Precursors for Microwave-Assisted and Thermal Conversion to Coordination Polymers with a High Influence on the Dielectric Properties. Chemistry. 2016 Feb 18;22(8):2708-18. doi: 10.1002/chem.201503725. Epub 2016 Jan 21. PMID: 26797710.
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Are intramolecular frustrated Lewis pairs also intramolecular catalysts? A theoretical study on H2 activation.

Physical chemistry chemical physics : PCCP

Zeonjuk LL, St Petkov P, Heine T, Röschenthaler GV, Eicher J, Vankova N.
PMID: 25812167
Phys Chem Chem Phys. 2015 Apr 28;17(16):10687-98. doi: 10.1039/c5cp00368g.

We investigate computationally a series of intramolecular frustrated Lewis pairs (FLPs), with the general formula Mes2PCHRCH2B(C6F5)2, that are known from the literature to either activate molecular hydrogen (FLPs with R = H (1) or Me (4)), or remain inert...

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Zeonjuk LL, St Petkov P, Heine T, et al. Are intramolecular frustrated Lewis pairs also intramolecular catalysts? A theoretical study on H2 activation. Phys Chem Chem Phys. 2015;17(16):10687-98doi: 10.1039/c5cp00368g.
Zeonjuk, L. L., St Petkov, P., Heine, T., Röschenthaler, G. V., Eicher, J., & Vankova, N. (2015). Are intramolecular frustrated Lewis pairs also intramolecular catalysts? A theoretical study on H2 activation. Physical chemistry chemical physics : PCCP, 17(16), 10687-98. https://doi.org/10.1039/c5cp00368g
Zeonjuk, Lei Liu, et al. "Are intramolecular frustrated Lewis pairs also intramolecular catalysts? A theoretical study on H2 activation." Physical chemistry chemical physics : PCCP vol. 17,16 (2015): 10687-98. doi: https://doi.org/10.1039/c5cp00368g
Zeonjuk LL, St Petkov P, Heine T, Röschenthaler GV, Eicher J, Vankova N. Are intramolecular frustrated Lewis pairs also intramolecular catalysts? A theoretical study on H2 activation. Phys Chem Chem Phys. 2015 Apr 28;17(16):10687-98. doi: 10.1039/c5cp00368g. PMID: 25812167.
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Showing 1 to 12 of 620 entries