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[Dresden public health efforts and their fate in the 1st half of the 20th century].

Zeitschrift fur die gesamte Hygiene und ihre Grenzgebiete

Heidel G.
PMID: 3326306
Z Gesamte Hyg. 1987 Nov;33(11):551-4.

No abstract available.

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Heidel G. Dresdener sozialhygienische Bemühungen und deren Schicksal in der ersten Hälfte des 20. Jahrhunderts. [Dresden public health efforts and their fate in the 1st half of the 20th century]. Z Gesamte Hyg. 1987;33(11):551-4
Heidel, G. (1987). Dresdener sozialhygienische Bemühungen und deren Schicksal in der ersten Hälfte des 20. Jahrhunderts. [Dresden public health efforts and their fate in the 1st half of the 20th century]. Zeitschrift fur die gesamte Hygiene und ihre Grenzgebiete, 33(11), 551-4.
Heidel, G. "Dresdener sozialhygienische Bemühungen und deren Schicksal in der ersten Hälfte des 20. Jahrhunderts." [Dresden public health efforts and their fate in the 1st half of the 20th century]. Zeitschrift fur die gesamte Hygiene und ihre Grenzgebiete vol. 33,11 (1987): 551-4.
Heidel G. Dresdener sozialhygienische Bemühungen und deren Schicksal in der ersten Hälfte des 20. Jahrhunderts. [Dresden public health efforts and their fate in the 1st half of the 20th century]. Z Gesamte Hyg. 1987 Nov;33(11):551-4. German. PMID: 3326306.
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Charge-transfer crystallites as molecular electrical dopants.

Nature communications

Méndez H, Heimel G, Winkler S, Frisch J, Opitz A, Sauer K, Wegner B, Oehzelt M, Röthel C, Duhm S, Többens D, Koch N, Salzmann I.
PMID: 26440403
Nat Commun. 2015 Oct 06;6:8560. doi: 10.1038/ncomms9560.

Ground-state integer charge transfer is commonly regarded as the basic mechanism of molecular electrical doping in both, conjugated polymers and oligomers. Here, we demonstrate that fundamentally different processes can occur in the two types of organic semiconductors instead. Using...

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Méndez H, Heimel G, Winkler S, et al. Charge-transfer crystallites as molecular electrical dopants. Nat Commun. 2015;6:8560doi: 10.1038/ncomms9560.
Méndez, H., Heimel, G., Winkler, S., Frisch, J., Opitz, A., Sauer, K., Wegner, B., Oehzelt, M., Röthel, C., Duhm, S., Többens, D., Koch, N., & Salzmann, I. (2015). Charge-transfer crystallites as molecular electrical dopants. Nature communications, 68560. https://doi.org/10.1038/ncomms9560
Méndez, Henry, et al. "Charge-transfer crystallites as molecular electrical dopants." Nature communications vol. 6 (2015): 8560. doi: https://doi.org/10.1038/ncomms9560
Méndez H, Heimel G, Winkler S, Frisch J, Opitz A, Sauer K, Wegner B, Oehzelt M, Röthel C, Duhm S, Többens D, Koch N, Salzmann I. Charge-transfer crystallites as molecular electrical dopants. Nat Commun. 2015 Oct 06;6:8560. doi: 10.1038/ncomms9560. PMID: 26440403; PMCID: PMC4600739.
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[The year 1989. A turning point for pathology at the University of Leipzig?].

Der Pathologe

Geiler G.
PMID: 11490936
Pathologe. 2001 Jul;22(4):235-40. doi: 10.1007/s002920000450.

No abstract available.

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Geiler G. Das Jahr 1989. Eine Wende auch für die Pathologie an der Universität Leipzig? [The year 1989. A turning point for pathology at the University of Leipzig?]. Pathologe. 2001;22(4):235-40doi: 10.1007/s002920000450.
Geiler, G. (2001). Das Jahr 1989. Eine Wende auch für die Pathologie an der Universität Leipzig? [The year 1989. A turning point for pathology at the University of Leipzig?]. Der Pathologe, 22(4), 235-40. https://doi.org/10.1007/s002920000450
Geiler, G. "Das Jahr 1989. Eine Wende auch für die Pathologie an der Universität Leipzig?" [The year 1989. A turning point for pathology at the University of Leipzig?]. Der Pathologe vol. 22,4 (2001): 235-40. doi: https://doi.org/10.1007/s002920000450
Geiler G. Das Jahr 1989. Eine Wende auch für die Pathologie an der Universität Leipzig? [The year 1989. A turning point for pathology at the University of Leipzig?]. Pathologe. 2001 Jul;22(4):235-40. doi: 10.1007/s002920000450. German. PMID: 11490936.
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Intramolecular charge transfer assisted by conformational changes in the excited state of fluorene-dibenzothiophene-S,S-dioxide co-oligomers.

The journal of physical chemistry. B

Dias FB, Pollock S, Hedley G, Pålsson LO, Monkman A, Perepichka II, Perepichka IF, Tavasli M, Bryce MR.
PMID: 17004789
J Phys Chem B. 2006 Oct 05;110(39):19329-39. doi: 10.1021/jp0643653.

The strong solvatochromism observed for two fluorene-dibenzothiophene-S,S-dioxide oligomers in polar solvents has been investigated using steady-state and time-resolved fluorescence techniques. A low-energy absorption band, attributed to a charge-transfer (CT) state, is identified by its red shift with increasing solvent...

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Dias FB, Pollock S, Hedley G, et al. Intramolecular charge transfer assisted by conformational changes in the excited state of fluorene-dibenzothiophene-S,S-dioxide co-oligomers. J Phys Chem B. 2006;110(39):19329-39doi: 10.1021/jp0643653.
Dias, F. B., Pollock, S., Hedley, G., Pålsson, L. O., Monkman, A., Perepichka, I. I., Perepichka, I. F., Tavasli, M., & Bryce, M. R. (2006). Intramolecular charge transfer assisted by conformational changes in the excited state of fluorene-dibenzothiophene-S,S-dioxide co-oligomers. The journal of physical chemistry. B, 110(39), 19329-39. https://doi.org/10.1021/jp0643653
Dias, Fernando B, et al. "Intramolecular charge transfer assisted by conformational changes in the excited state of fluorene-dibenzothiophene-S,S-dioxide co-oligomers." The journal of physical chemistry. B vol. 110,39 (2006): 19329-39. doi: https://doi.org/10.1021/jp0643653
Dias FB, Pollock S, Hedley G, Pålsson LO, Monkman A, Perepichka II, Perepichka IF, Tavasli M, Bryce MR. Intramolecular charge transfer assisted by conformational changes in the excited state of fluorene-dibenzothiophene-S,S-dioxide co-oligomers. J Phys Chem B. 2006 Oct 05;110(39):19329-39. doi: 10.1021/jp0643653. PMID: 17004789.
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Odd-even effects in self-assembled monolayers of omega-(biphenyl-4-yl)alkanethiols: a first-principles study.

Langmuir : the ACS journal of surfaces and colloids

Heimel G, Romaner L, Brédas JL, Zojer E.
PMID: 18072797
Langmuir. 2008 Jan 15;24(2):474-82. doi: 10.1021/la7023814. Epub 2007 Dec 12.

Conjugated molecules with a saturated alkyl linker between a thiol docking group and the pi-conjugated core have been shown to form self-assembled monolayers (SAMs) with a high degree of long-range order and uniformity. Additionally, pronounced odd-even effects have been...

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Heimel G, Romaner L, Brédas JL, et al. Odd-even effects in self-assembled monolayers of omega-(biphenyl-4-yl)alkanethiols: a first-principles study. Langmuir. 2007;24(2):474-82doi: 10.1021/la7023814.
Heimel, G., Romaner, L., Brédas, J. L., & Zojer, E. (2008). Odd-even effects in self-assembled monolayers of omega-(biphenyl-4-yl)alkanethiols: a first-principles study. Langmuir : the ACS journal of surfaces and colloids, 24(2), 474-82. https://doi.org/10.1021/la7023814
Heimel, Georg, et al. "Odd-even effects in self-assembled monolayers of omega-(biphenyl-4-yl)alkanethiols: a first-principles study." Langmuir : the ACS journal of surfaces and colloids vol. 24,2 (2008): 474-82. doi: https://doi.org/10.1021/la7023814
Heimel G, Romaner L, Brédas JL, Zojer E. Odd-even effects in self-assembled monolayers of omega-(biphenyl-4-yl)alkanethiols: a first-principles study. Langmuir. 2008 Jan 15;24(2):474-82. doi: 10.1021/la7023814. Epub 2007 Dec 12. PMID: 18072797.
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Pulsar NP 0532: properties and systematic polarization of individual strong pulses at 430 MHz.

Nature

Heiles C, Campbell DB, Rankin JM.
PMID: 16057371
Nature. 1970 May 09;226(5245):529-31. doi: 10.1038/226529a0.

This paper reports further detailed measurements of strong radio pulses from the pulsar NP 0532 in the Crab nebula, recorded at Arecibo.

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Heiles C, Campbell DB, Rankin JM. Pulsar NP 0532: properties and systematic polarization of individual strong pulses at 430 MHz. Nature. 1970;226(5245):529-31doi: 10.1038/226529a0.
Heiles, C., Campbell, D. B., & Rankin, J. M. (1970). Pulsar NP 0532: properties and systematic polarization of individual strong pulses at 430 MHz. Nature, 226(5245), 529-31. https://doi.org/10.1038/226529a0
Heiles, C, et al. "Pulsar NP 0532: properties and systematic polarization of individual strong pulses at 430 MHz." Nature vol. 226,5245 (1970): 529-31. doi: https://doi.org/10.1038/226529a0
Heiles C, Campbell DB, Rankin JM. Pulsar NP 0532: properties and systematic polarization of individual strong pulses at 430 MHz. Nature. 1970 May 09;226(5245):529-31. doi: 10.1038/226529a0. PMID: 16057371.
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Tuning the ionization energy of organic semiconductor films: the role of intramolecular polar bonds.

Journal of the American Chemical Society

Salzmann I, Duhm S, Heimel G, Oehzelt M, Kniprath R, Johnson RL, Rabe JP, Koch N.
PMID: 18771262
J Am Chem Soc. 2008 Oct 01;130(39):12870-1. doi: 10.1021/ja804793a. Epub 2008 Sep 05.

For the prototypical conjugated organic molecules pentacene and perfluoropentacene, we demonstrate that the surface termination of ordered organic thin films with intramolecular polar bonds (e.g., -H versus -F) can be used to tune the ionization energy. The collective electrostatics...

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Salzmann I, Duhm S, Heimel G, et al. Tuning the ionization energy of organic semiconductor films: the role of intramolecular polar bonds. J Am Chem Soc. 2008;130(39):12870-1doi: 10.1021/ja804793a.
Salzmann, I., Duhm, S., Heimel, G., Oehzelt, M., Kniprath, R., Johnson, R. L., Rabe, J. P., & Koch, N. (2008). Tuning the ionization energy of organic semiconductor films: the role of intramolecular polar bonds. Journal of the American Chemical Society, 130(39), 12870-1. https://doi.org/10.1021/ja804793a
Salzmann, Ingo, et al. "Tuning the ionization energy of organic semiconductor films: the role of intramolecular polar bonds." Journal of the American Chemical Society vol. 130,39 (2008): 12870-1. doi: https://doi.org/10.1021/ja804793a
Salzmann I, Duhm S, Heimel G, Oehzelt M, Kniprath R, Johnson RL, Rabe JP, Koch N. Tuning the ionization energy of organic semiconductor films: the role of intramolecular polar bonds. J Am Chem Soc. 2008 Oct 01;130(39):12870-1. doi: 10.1021/ja804793a. Epub 2008 Sep 05. PMID: 18771262.
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Feature extraction for texture discrimination via random field models with random spatial interaction.

IEEE transactions on image processing : a publication of the IEEE Signal Processing Society

Speis A, Healey G.
PMID: 18285151
IEEE Trans Image Process. 1996;5(4):635-45. doi: 10.1109/83.491339.

In this paper, we attack the problem of distinguishing textured images of real surfaces using small samples. We first analyze experimental data that results from applying ordinary conditional Markov fields. In the face of the disappointing performance of these...

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Speis A, Healey G. Feature extraction for texture discrimination via random field models with random spatial interaction. IEEE Trans Image Process. 1996;5(4):635-45doi: 10.1109/83.491339.
Speis, A., & Healey, G. (1996). Feature extraction for texture discrimination via random field models with random spatial interaction. IEEE transactions on image processing : a publication of the IEEE Signal Processing Society, 5(4), 635-45. https://doi.org/10.1109/83.491339
Speis, A, and Healey, G. "Feature extraction for texture discrimination via random field models with random spatial interaction." IEEE transactions on image processing : a publication of the IEEE Signal Processing Society vol. 5,4 (1996): 635-45. doi: https://doi.org/10.1109/83.491339
Speis A, Healey G. Feature extraction for texture discrimination via random field models with random spatial interaction. IEEE Trans Image Process. 1996;5(4):635-45. doi: 10.1109/83.491339. PMID: 18285151.
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Orientation-dependent ionization energies and interface dipoles in ordered molecular assemblies.

Nature materials

Duhm S, Heimel G, Salzmann I, Glowatzki H, Johnson RL, Vollmer A, Rabe JP, Koch N.
PMID: 18264103
Nat Mater. 2008 Apr;7(4):326-32. doi: 10.1038/nmat2119. Epub 2008 Feb 10.

Although an isolated individual molecule clearly has only one ionization potential, multiple values are found for molecules in ordered assemblies. Photoelectron spectroscopy of archetypical pi-conjugated organic compounds on metal substrates combined with first-principles calculations and electrostatic modelling reveal the...

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Duhm S, Heimel G, Salzmann I, et al. Orientation-dependent ionization energies and interface dipoles in ordered molecular assemblies. Nat Mater. 2008;7(4):326-32doi: 10.1038/nmat2119.
Duhm, S., Heimel, G., Salzmann, I., Glowatzki, H., Johnson, R. L., Vollmer, A., Rabe, J. P., & Koch, N. (2008). Orientation-dependent ionization energies and interface dipoles in ordered molecular assemblies. Nature materials, 7(4), 326-32. https://doi.org/10.1038/nmat2119
Duhm, Steffen, et al. "Orientation-dependent ionization energies and interface dipoles in ordered molecular assemblies." Nature materials vol. 7,4 (2008): 326-32. doi: https://doi.org/10.1038/nmat2119
Duhm S, Heimel G, Salzmann I, Glowatzki H, Johnson RL, Vollmer A, Rabe JP, Koch N. Orientation-dependent ionization energies and interface dipoles in ordered molecular assemblies. Nat Mater. 2008 Apr;7(4):326-32. doi: 10.1038/nmat2119. Epub 2008 Feb 10. PMID: 18264103.
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Note: gas phase structures of bare Si8 and Si11 clusters from molecular beam electric deflection experiments.

The Journal of chemical physics

Götz DA, Heiles S, Johnston RL, Schäfer R.
PMID: 22583313
J Chem Phys. 2012 May 14;136(18):186101. doi: 10.1063/1.4717708.

No abstract available.

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Götz DA, Heiles S, Johnston RL, et al. Note: gas phase structures of bare Si8 and Si11 clusters from molecular beam electric deflection experiments. J Chem Phys. 2012;136(18):186101doi: 10.1063/1.4717708.
Götz, D. A., Heiles, S., Johnston, R. L., & Schäfer, R. (2012). Note: gas phase structures of bare Si8 and Si11 clusters from molecular beam electric deflection experiments. The Journal of chemical physics, 136(18), 186101. https://doi.org/10.1063/1.4717708
Götz, D A, et al. "Note: gas phase structures of bare Si8 and Si11 clusters from molecular beam electric deflection experiments." The Journal of chemical physics vol. 136,18 (2012): 186101. doi: https://doi.org/10.1063/1.4717708
Götz DA, Heiles S, Johnston RL, Schäfer R. Note: gas phase structures of bare Si8 and Si11 clusters from molecular beam electric deflection experiments. J Chem Phys. 2012 May 14;136(18):186101. doi: 10.1063/1.4717708. PMID: 22583313.
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New Reactor Design for Photocatalytic Wastewater Treatment with TiO2 Immobilized on Fused-Silica Glass Fibers: Photomineralization of 4-Chlorophenol.

Environmental science & technology

Hofstadler K, Bauer R, Novalic S, Heisler G.
PMID: 22196551
Environ Sci Technol. 1994 Apr 01;28(4):670-4. doi: 10.1021/es00053a021.

No abstract available.

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Hofstadler K, Bauer R, Novalic S, et al. New Reactor Design for Photocatalytic Wastewater Treatment with TiO2 Immobilized on Fused-Silica Glass Fibers: Photomineralization of 4-Chlorophenol. Environ Sci Technol. 1994;28(4):670-4doi: 10.1021/es00053a021.
Hofstadler, K., Bauer, R., Novalic, S., & Heisler, G. (1994). New Reactor Design for Photocatalytic Wastewater Treatment with TiO2 Immobilized on Fused-Silica Glass Fibers: Photomineralization of 4-Chlorophenol. Environmental science & technology, 28(4), 670-4. https://doi.org/10.1021/es00053a021
Hofstadler, K, et al. "New Reactor Design for Photocatalytic Wastewater Treatment with TiO2 Immobilized on Fused-Silica Glass Fibers: Photomineralization of 4-Chlorophenol." Environmental science & technology vol. 28,4 (1994): 670-4. doi: https://doi.org/10.1021/es00053a021
Hofstadler K, Bauer R, Novalic S, Heisler G. New Reactor Design for Photocatalytic Wastewater Treatment with TiO2 Immobilized on Fused-Silica Glass Fibers: Photomineralization of 4-Chlorophenol. Environ Sci Technol. 1994 Apr 01;28(4):670-4. doi: 10.1021/es00053a021. PMID: 22196551.
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On the rotational temperature and structure dependence of electric field deflection experiments: a case study of germanium clusters.

The Journal of chemical physics

Heiles S, Schäfer S, Schäfer R.
PMID: 21786999
J Chem Phys. 2011 Jul 21;135(3):034303. doi: 10.1063/1.3610390.

Molecular beam electric field deflection experiments offer a probe to the structural and dielectric properties of isolated particles in the gas phase. However, their quantitative interpretation is still a formidable task. Despite the benefits of this method, the analysis...

Cite
Heiles S, Schäfer S, Schäfer R. On the rotational temperature and structure dependence of electric field deflection experiments: a case study of germanium clusters. J Chem Phys. 2011;135(3):034303doi: 10.1063/1.3610390.
Heiles, S., Schäfer, S., & Schäfer, R. (2011). On the rotational temperature and structure dependence of electric field deflection experiments: a case study of germanium clusters. The Journal of chemical physics, 135(3), 034303. https://doi.org/10.1063/1.3610390
Heiles, S, et al. "On the rotational temperature and structure dependence of electric field deflection experiments: a case study of germanium clusters." The Journal of chemical physics vol. 135,3 (2011): 034303. doi: https://doi.org/10.1063/1.3610390
Heiles S, Schäfer S, Schäfer R. On the rotational temperature and structure dependence of electric field deflection experiments: a case study of germanium clusters. J Chem Phys. 2011 Jul 21;135(3):034303. doi: 10.1063/1.3610390. PMID: 21786999.
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Showing 1 to 12 of 153 entries