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Showing 1 to 12 of 91 entries
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Core Halogenation as a Construction Principle in Tuning the Material Properties of Tetraazaperopyrenes.

Chemistry (Weinheim an der Bergstrasse, Germany)

Hahn L, Maass F, Bleith T, Zschieschang U, Wadepohl H, Klauk H, Tegeder P, Gade LH.
PMID: 26507207
Chemistry. 2015 Dec 01;21(49):17691-700. doi: 10.1002/chem.201503484. Epub 2015 Oct 28.

A detailed study on the effects of core halogenation of tetraazaperopyrene (TAPP) derivatives is presented. Its impact on the solid structure, as well as the photophysical and electrochemical properties, has been probed by the means of X-ray crystallography, UV/Vis...

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Hahn L, Maass F, Bleith T, et al. Core Halogenation as a Construction Principle in Tuning the Material Properties of Tetraazaperopyrenes. Chemistry. 2015;21(49):17691-700doi: 10.1002/chem.201503484.
Hahn, L., Maass, F., Bleith, T., Zschieschang, U., Wadepohl, H., Klauk, H., Tegeder, P., & Gade, L. H. (2015). Core Halogenation as a Construction Principle in Tuning the Material Properties of Tetraazaperopyrenes. Chemistry (Weinheim an der Bergstrasse, Germany), 21(49), 17691-700. https://doi.org/10.1002/chem.201503484
Hahn, Lena, et al. "Core Halogenation as a Construction Principle in Tuning the Material Properties of Tetraazaperopyrenes." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,49 (2015): 17691-700. doi: https://doi.org/10.1002/chem.201503484
Hahn L, Maass F, Bleith T, Zschieschang U, Wadepohl H, Klauk H, Tegeder P, Gade LH. Core Halogenation as a Construction Principle in Tuning the Material Properties of Tetraazaperopyrenes. Chemistry. 2015 Dec 01;21(49):17691-700. doi: 10.1002/chem.201503484. Epub 2015 Oct 28. PMID: 26507207.
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Nonlinear optical response of photochromic azobenzene-functionalized self-assembled monolayers.

Physical chemistry chemical physics : PCCP

Schulze M, Utecht M, Moldt T, Przyrembel D, Gahl C, Weinelt M, Saalfrank P, Tegeder P.
PMID: 26100382
Phys Chem Chem Phys. 2015 Jul 21;17(27):18079-86. doi: 10.1039/c5cp03093e. Epub 2015 Jun 23.

The combination of photochromic and nonlinear optical (NLO) properties of azobenzene-functionalized self-assembled monolayers (SAMs) constitutes an intriguing step towards novel photonic and optoelectronic devices. By utilizing the second-order NLO process of second harmonic generation (SHG), supported by density-functional theory...

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Schulze M, Utecht M, Moldt T, et al. Nonlinear optical response of photochromic azobenzene-functionalized self-assembled monolayers. Phys Chem Chem Phys. 2015;17(27):18079-86doi: 10.1039/c5cp03093e.
Schulze, M., Utecht, M., Moldt, T., Przyrembel, D., Gahl, C., Weinelt, M., Saalfrank, P., & Tegeder, P. (2015). Nonlinear optical response of photochromic azobenzene-functionalized self-assembled monolayers. Physical chemistry chemical physics : PCCP, 17(27), 18079-86. https://doi.org/10.1039/c5cp03093e
Schulze, Michael, et al. "Nonlinear optical response of photochromic azobenzene-functionalized self-assembled monolayers." Physical chemistry chemical physics : PCCP vol. 17,27 (2015): 18079-86. doi: https://doi.org/10.1039/c5cp03093e
Schulze M, Utecht M, Moldt T, Przyrembel D, Gahl C, Weinelt M, Saalfrank P, Tegeder P. Nonlinear optical response of photochromic azobenzene-functionalized self-assembled monolayers. Phys Chem Chem Phys. 2015 Jul 21;17(27):18079-86. doi: 10.1039/c5cp03093e. Epub 2015 Jun 23. PMID: 26100382.
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Isolation and characterization of muscle fatigue substance with anti-tumor activities.

Journal of Cancer

Munoz RM, Han H, Tegeler T, Petritis K, Von Hoff DD, Hoffman SA.
PMID: 23678371
J Cancer. 2013 May 09;4(4):343-9. doi: 10.7150/jca.5418. Print 2013.

Research during the 1950's indicated that exercise played a role in the reduction of tumor growth. In the 1960's our studies confirmed that tumor-bearing rats, exercised to fatigue, demonstrated tumor inhibition. Our further studies isolated an extract (Fatigue Substance,...

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Munoz RM, Han H, Tegeler T, et al. Isolation and characterization of muscle fatigue substance with anti-tumor activities. J Cancer. 2013;4(4):343-9doi: 10.7150/jca.5418.
Munoz, R. M., Han, H., Tegeler, T., Petritis, K., Von Hoff, D. D., & Hoffman, S. A. (2013). Isolation and characterization of muscle fatigue substance with anti-tumor activities. Journal of Cancer, 4(4), 343-9. https://doi.org/10.7150/jca.5418
Munoz, Ruben M, et al. "Isolation and characterization of muscle fatigue substance with anti-tumor activities." Journal of Cancer vol. 4,4 (2013): 343-9. doi: https://doi.org/10.7150/jca.5418
Munoz RM, Han H, Tegeler T, Petritis K, Von Hoff DD, Hoffman SA. Isolation and characterization of muscle fatigue substance with anti-tumor activities. J Cancer. 2013 May 09;4(4):343-9. doi: 10.7150/jca.5418. Print 2013. PMID: 23678371; PMCID: PMC3654491.
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Constant pH Molecular Dynamics in Explicit Solvent with λ-Dynamics.

Journal of chemical theory and computation

Donnini S, Tegeler F, Groenhof G, Grubmüller H.
PMID: 21687785
J Chem Theory Comput. 2011 Jun 14;7(6):1962-1978. doi: 10.1021/ct200061r. Epub 2011 Apr 25.

pH is an important parameter in condensed-phase systems, because it determines the protonation state of titratable groups and thus influences the structure, dynamics, and function of molecules in solution. In most force field simulation protocols, however, the protonation state...

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Donnini S, Tegeler F, Groenhof G, et al. Constant pH Molecular Dynamics in Explicit Solvent with λ-Dynamics. J Chem Theory Comput. 2011;7(6):1962-1978doi: 10.1021/ct200061r.
Donnini, S., Tegeler, F., Groenhof, G., & Grubmüller, H. (2011). Constant pH Molecular Dynamics in Explicit Solvent with λ-Dynamics. Journal of chemical theory and computation, 7(6), 1962-1978. https://doi.org/10.1021/ct200061r
Donnini, Serena, et al. "Constant pH Molecular Dynamics in Explicit Solvent with λ-Dynamics." Journal of chemical theory and computation vol. 7,6 (2011): 1962-1978. doi: https://doi.org/10.1021/ct200061r
Donnini S, Tegeler F, Groenhof G, Grubmüller H. Constant pH Molecular Dynamics in Explicit Solvent with λ-Dynamics. J Chem Theory Comput. 2011 Jun 14;7(6):1962-1978. doi: 10.1021/ct200061r. Epub 2011 Apr 25. PMID: 21687785; PMCID: PMC3114466.
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BRV-continuum source as a radiometric transfer standard between 40 nm and 600 nm.

Applied optics

Kühne M, Stuck D, Tegeler E.
PMID: 20396340
Appl Opt. 1982 Nov 01;21(21):3919-22. doi: 10.1364/AO.21.003919.

The BRV-continuum source was investigated for its potential use as a radiometric transfer standard in the wavelength region from 40 to 600 nm. Variations of the spectral radiance from one pulse to the other up to a factor of...

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Kühne M, Stuck D, Tegeler E. BRV-continuum source as a radiometric transfer standard between 40 nm and 600 nm. Appl Opt. 1982;21(21):3919-22doi: 10.1364/AO.21.003919.
Kühne, M., Stuck, D., & Tegeler, E. (1982). BRV-continuum source as a radiometric transfer standard between 40 nm and 600 nm. Applied optics, 21(21), 3919-22. https://doi.org/10.1364/AO.21.003919
Kühne, M, et al. "BRV-continuum source as a radiometric transfer standard between 40 nm and 600 nm." Applied optics vol. 21,21 (1982): 3919-22. doi: https://doi.org/10.1364/AO.21.003919
Kühne M, Stuck D, Tegeler E. BRV-continuum source as a radiometric transfer standard between 40 nm and 600 nm. Appl Opt. 1982 Nov 01;21(21):3919-22. doi: 10.1364/AO.21.003919. PMID: 20396340.
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Adsorption energetics of azobenzenes on noble metal surfaces.

Journal of physics. Condensed matter : an Institute of Physics journal

Schulze M, Bronner C, Tegeder P.
PMID: 25077738
J Phys Condens Matter. 2014 Sep 03;26(35):355004. doi: 10.1088/0953-8984/26/35/355004. Epub 2014 Jul 31.

Temperature-programmed desorption measurements have been applied to investigate the binding energies of four systems, namely the photochromic molecular compounds azobenzene and tetra-tert-butyl-azobenzene (TBA) adsorbed on the Au(1 1 1) and Ag(1 1 1) surfaces, respectively. The binding energy is...

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Schulze M, Bronner C, Tegeder P. Adsorption energetics of azobenzenes on noble metal surfaces. J Phys Condens Matter. 2014;26(35):355004doi: 10.1088/0953-8984/26/35/355004.
Schulze, M., Bronner, C., & Tegeder, P. (2014). Adsorption energetics of azobenzenes on noble metal surfaces. Journal of physics. Condensed matter : an Institute of Physics journal, 26(35), 355004. https://doi.org/10.1088/0953-8984/26/35/355004
Schulze, Michael, et al. "Adsorption energetics of azobenzenes on noble metal surfaces." Journal of physics. Condensed matter : an Institute of Physics journal vol. 26,35 (2014): 355004. doi: https://doi.org/10.1088/0953-8984/26/35/355004
Schulze M, Bronner C, Tegeder P. Adsorption energetics of azobenzenes on noble metal surfaces. J Phys Condens Matter. 2014 Sep 03;26(35):355004. doi: 10.1088/0953-8984/26/35/355004. Epub 2014 Jul 31. PMID: 25077738.
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Molecular Ion Formation by Photoinduced Electron Transfer at the Tetracyanoquinodimethane/Au(111) Interface.

The journal of physical chemistry letters

Gerbert D, Tegeder P.
PMID: 28899087
J Phys Chem Lett. 2017 Oct 05;8(19):4685-4690. doi: 10.1021/acs.jpclett.7b01897. Epub 2017 Sep 15.

Optically induced processes in organic materials are essential for light harvesting, switching, and sensor technologies. Here we studied the electronic properties of the tetracyanoquinodimethane(TCNQ)/Au(111) interface by using two-photon photoemission spectroscopy. For this interface we demonstrated the lack of charge-transfer...

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Gerbert D, Tegeder P. Molecular Ion Formation by Photoinduced Electron Transfer at the Tetracyanoquinodimethane/Au(111) Interface. J Phys Chem Lett. 2017;8(19):4685-4690doi: 10.1021/acs.jpclett.7b01897.
Gerbert, D., & Tegeder, P. (2017). Molecular Ion Formation by Photoinduced Electron Transfer at the Tetracyanoquinodimethane/Au(111) Interface. The journal of physical chemistry letters, 8(19), 4685-4690. https://doi.org/10.1021/acs.jpclett.7b01897
Gerbert, David, and Tegeder, Petra. "Molecular Ion Formation by Photoinduced Electron Transfer at the Tetracyanoquinodimethane/Au(111) Interface." The journal of physical chemistry letters vol. 8,19 (2017): 4685-4690. doi: https://doi.org/10.1021/acs.jpclett.7b01897
Gerbert D, Tegeder P. Molecular Ion Formation by Photoinduced Electron Transfer at the Tetracyanoquinodimethane/Au(111) Interface. J Phys Chem Lett. 2017 Oct 05;8(19):4685-4690. doi: 10.1021/acs.jpclett.7b01897. Epub 2017 Sep 15. PMID: 28899087.
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Reversible end-to-end assembly of selectively functionalized gold nanorods by light-responsive arylazopyrazole-cyclodextrin interaction.

Beilstein journal of organic chemistry

Niehues M, Tegeder P, Ravoo BJ.
PMID: 31293690
Beilstein J Org Chem. 2019 Jun 26;15:1407-1415. doi: 10.3762/bjoc.15.140. eCollection 2019.

We propose a two-step ligand exchange for the selective end-functionalization of gold nanorods (AuNR) by thiolated cyclodextrin (CD) host molecules. As a result of the complete removal of the precursor capping agent cetyltrimethylammonium bromide (CTAB) by a tetraethylene glycol...

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Niehues M, Tegeder P, Ravoo BJ. Reversible end-to-end assembly of selectively functionalized gold nanorods by light-responsive arylazopyrazole-cyclodextrin interaction. Beilstein J Org Chem. 2019;15:1407-1415doi: 10.3762/bjoc.15.140.
Niehues, M., Tegeder, P., & Ravoo, B. J. (2019). Reversible end-to-end assembly of selectively functionalized gold nanorods by light-responsive arylazopyrazole-cyclodextrin interaction. Beilstein journal of organic chemistry, 151407-1415. https://doi.org/10.3762/bjoc.15.140
Niehues, Maximilian, et al. "Reversible end-to-end assembly of selectively functionalized gold nanorods by light-responsive arylazopyrazole-cyclodextrin interaction." Beilstein journal of organic chemistry vol. 15 (2019): 1407-1415. doi: https://doi.org/10.3762/bjoc.15.140
Niehues M, Tegeder P, Ravoo BJ. Reversible end-to-end assembly of selectively functionalized gold nanorods by light-responsive arylazopyrazole-cyclodextrin interaction. Beilstein J Org Chem. 2019 Jun 26;15:1407-1415. doi: 10.3762/bjoc.15.140. eCollection 2019. PMID: 31293690; PMCID: PMC6604721.
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Electronic structure of an iron porphyrin derivative on Au(1 1 1).

Journal of physics. Condensed matter : an Institute of Physics journal

Stein A, Rolf D, Lotze C, Czekelius C, Franke KJ, Tegeder P.
PMID: 30523801
J Phys Condens Matter. 2019 Jan 30;31(4):044002. doi: 10.1088/1361-648X/aaf296. Epub 2018 Nov 21.

Surface-bound porphyrins are promising candidates for molecular switches, electronics and spintronics. Here, we studied the structural and the electronic properties of Fe-tetra-pyridil-porphyrin adsorbed on Au(1 1 1) in the monolayer regime. We combined scanning tunneling microscopy/spectroscopy, ultraviolet photoemission, and...

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Stein A, Rolf D, Lotze C, et al. Electronic structure of an iron porphyrin derivative on Au(1 1 1). J Phys Condens Matter. 2018;31(4):044002doi: 10.1088/1361-648X/aaf296.
Stein, A., Rolf, D., Lotze, C., Czekelius, C., Franke, K. J., & Tegeder, P. (2019). Electronic structure of an iron porphyrin derivative on Au(1 1 1). Journal of physics. Condensed matter : an Institute of Physics journal, 31(4), 044002. https://doi.org/10.1088/1361-648X/aaf296
Stein, Arnulf, et al. "Electronic structure of an iron porphyrin derivative on Au(1 1 1)." Journal of physics. Condensed matter : an Institute of Physics journal vol. 31,4 (2019): 044002. doi: https://doi.org/10.1088/1361-648X/aaf296
Stein A, Rolf D, Lotze C, Czekelius C, Franke KJ, Tegeder P. Electronic structure of an iron porphyrin derivative on Au(1 1 1). J Phys Condens Matter. 2019 Jan 30;31(4):044002. doi: 10.1088/1361-648X/aaf296. Epub 2018 Nov 21. PMID: 30523801.
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Binding energies of benzene on coinage metal surfaces: Equal stability on different metals.

The Journal of chemical physics

Maaß F, Jiang Y, Liu W, Tkatchenko A, Tegeder P.
PMID: 29884059
J Chem Phys. 2018 Jun 07;148(21):214703. doi: 10.1063/1.5030094.

Interfaces between organic molecules and inorganic solids adapt a prominent role in fundamental science, catalysis, molecular sensors, and molecular electronics. The molecular adsorption geometry, which is dictated by the strength of lateral and vertical interactions, determines the electronic structure...

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Maaß F, Jiang Y, Liu W, et al. Binding energies of benzene on coinage metal surfaces: Equal stability on different metals. J Chem Phys. 2018;148(21):214703doi: 10.1063/1.5030094.
Maaß, F., Jiang, Y., Liu, W., Tkatchenko, A., & Tegeder, P. (2018). Binding energies of benzene on coinage metal surfaces: Equal stability on different metals. The Journal of chemical physics, 148(21), 214703. https://doi.org/10.1063/1.5030094
Maaß, Friedrich, et al. "Binding energies of benzene on coinage metal surfaces: Equal stability on different metals." The Journal of chemical physics vol. 148,21 (2018): 214703. doi: https://doi.org/10.1063/1.5030094
Maaß F, Jiang Y, Liu W, Tkatchenko A, Tegeder P. Binding energies of benzene on coinage metal surfaces: Equal stability on different metals. J Chem Phys. 2018 Jun 07;148(21):214703. doi: 10.1063/1.5030094. PMID: 29884059.
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Band Formation at Interfaces Between N-Heteropolycycles and Gold Electrodes.

The journal of physical chemistry letters

Stein A, Rolf D, Lotze C, Günther B, Gade LH, Franke KJ, Tegeder P.
PMID: 33440118
J Phys Chem Lett. 2021 Jan 21;12(2):947-951. doi: 10.1021/acs.jpclett.0c03630. Epub 2021 Jan 13.

Efficient charge injection at organic semiconductor/metal interfaces is crucial for the performance of organic field effect transistors. Interfacial hybrid band formation between electronic states of the organic compound and the metal electrode facilitates effective charge injection. Here, we show...

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Stein A, Rolf D, Lotze C, et al. Band Formation at Interfaces Between N-Heteropolycycles and Gold Electrodes. J Phys Chem Lett. 2021;12(2):947-951doi: 10.1021/acs.jpclett.0c03630.
Stein, A., Rolf, D., Lotze, C., Günther, B., Gade, L. H., Franke, K. J., & Tegeder, P. (2021). Band Formation at Interfaces Between N-Heteropolycycles and Gold Electrodes. The journal of physical chemistry letters, 12(2), 947-951. https://doi.org/10.1021/acs.jpclett.0c03630
Stein, Arnulf, et al. "Band Formation at Interfaces Between N-Heteropolycycles and Gold Electrodes." The journal of physical chemistry letters vol. 12,2 (2021): 947-951. doi: https://doi.org/10.1021/acs.jpclett.0c03630
Stein A, Rolf D, Lotze C, Günther B, Gade LH, Franke KJ, Tegeder P. Band Formation at Interfaces Between N-Heteropolycycles and Gold Electrodes. J Phys Chem Lett. 2021 Jan 21;12(2):947-951. doi: 10.1021/acs.jpclett.0c03630. Epub 2021 Jan 13. PMID: 33440118.
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Altering ureide transport in nodulated soybean results in whole-plant adjustments of metabolism, assimilate partitioning, and sink strength.

Journal of plant physiology

Lu MZ, Carter AM, Tegeder M.
PMID: 35033961
J Plant Physiol. 2021 Dec 28;269:153613. doi: 10.1016/j.jplph.2021.153613. Epub 2021 Dec 28.

Legumes develop a symbiotic relationship with bacteria that are housed in root nodules and fix atmospheric di-nitrogen (N

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Lu MZ, Carter AM, Tegeder M. Altering ureide transport in nodulated soybean results in whole-plant adjustments of metabolism, assimilate partitioning, and sink strength. J Plant Physiol. 2021;269:153613doi: 10.1016/j.jplph.2021.153613.
Lu, M. Z., Carter, A. M., & Tegeder, M. (2021). Altering ureide transport in nodulated soybean results in whole-plant adjustments of metabolism, assimilate partitioning, and sink strength. Journal of plant physiology, 269153613. https://doi.org/10.1016/j.jplph.2021.153613
Lu, Ming-Zhu, et al. "Altering ureide transport in nodulated soybean results in whole-plant adjustments of metabolism, assimilate partitioning, and sink strength." Journal of plant physiology vol. 269 (2021): 153613. doi: https://doi.org/10.1016/j.jplph.2021.153613
Lu MZ, Carter AM, Tegeder M. Altering ureide transport in nodulated soybean results in whole-plant adjustments of metabolism, assimilate partitioning, and sink strength. J Plant Physiol. 2021 Dec 28;269:153613. doi: 10.1016/j.jplph.2021.153613. Epub 2021 Dec 28. PMID: 35033961.
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Showing 1 to 12 of 91 entries