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NMR studies of dilithiostyrenes: aggregation, NMR parameters, and DFT calculations for (E)-1-Lithio-2-(o-lithiophenyl)-1-trimethylsilylethene.

Magnetic resonance in chemistry : MRC

Böhler B, Günther H, Reider K, Maercker A, Gerbig D, Hausmann H.
PMID: 26249216
Magn Reson Chem. 2017 Mar;55(3):183-190. doi: 10.1002/mrc.4298. Epub 2015 Aug 06.

The dilithio compound (E)-1-lithio-2-(o-lithiophenyl)-1-trimethylsilylethene (5) was synthesized from 2-trimethylsilylbenzo-[b]tellurophene (6) with lithium-6 and a detailed analysis of its

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Böhler B, Günther H, Reider K, et al. NMR studies of dilithiostyrenes: aggregation, NMR parameters, and DFT calculations for (E)-1-Lithio-2-(o-lithiophenyl)-1-trimethylsilylethene. Magn Reson Chem. 2015;55(3):183-190doi: 10.1002/mrc.4298.
Böhler, B., Günther, H., Reider, K., Maercker, A., Gerbig, D., & Hausmann, H. (2017). NMR studies of dilithiostyrenes: aggregation, NMR parameters, and DFT calculations for (E)-1-Lithio-2-(o-lithiophenyl)-1-trimethylsilylethene. Magnetic resonance in chemistry : MRC, 55(3), 183-190. https://doi.org/10.1002/mrc.4298
Böhler, Bernd, et al. "NMR studies of dilithiostyrenes: aggregation, NMR parameters, and DFT calculations for (E)-1-Lithio-2-(o-lithiophenyl)-1-trimethylsilylethene." Magnetic resonance in chemistry : MRC vol. 55,3 (2017): 183-190. doi: https://doi.org/10.1002/mrc.4298
Böhler B, Günther H, Reider K, Maercker A, Gerbig D, Hausmann H. NMR studies of dilithiostyrenes: aggregation, NMR parameters, and DFT calculations for (E)-1-Lithio-2-(o-lithiophenyl)-1-trimethylsilylethene. Magn Reson Chem. 2017 Mar;55(3):183-190. doi: 10.1002/mrc.4298. Epub 2015 Aug 06. PMID: 26249216.
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Mechanism by which noninhibitory concentrations of glucose increase inhibitory activity ofp-coumaric acid on morning-glory seedling biomass accumulation.

Journal of chemical ecology

Pue KJ, Blum U, Gerig TM, Shafer SR.
PMID: 24234321
J Chem Ecol. 1995 Jun;21(6):833-47. doi: 10.1007/BF02033464.

Noninhibitory levels of glucose-C [≤ 72 µg carbon (C)/g soil] increased the inhibitory activity ofp-coumaric acid on morning-glory seedling biomass accumulation in Cecil Bt-horizon soil. The amount ofp-coumaric acid required for a given level of inhibition of shoot and...

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Pue KJ, Blum U, Gerig TM, et al. Mechanism by which noninhibitory concentrations of glucose increase inhibitory activity ofp-coumaric acid on morning-glory seedling biomass accumulation. J Chem Ecol. 1995;21(6):833-47doi: 10.1007/BF02033464.
Pue, K. J., Blum, U., Gerig, T. M., & Shafer, S. R. (1995). Mechanism by which noninhibitory concentrations of glucose increase inhibitory activity ofp-coumaric acid on morning-glory seedling biomass accumulation. Journal of chemical ecology, 21(6), 833-47. https://doi.org/10.1007/BF02033464
Pue, K J, et al. "Mechanism by which noninhibitory concentrations of glucose increase inhibitory activity ofp-coumaric acid on morning-glory seedling biomass accumulation." Journal of chemical ecology vol. 21,6 (1995): 833-47. doi: https://doi.org/10.1007/BF02033464
Pue KJ, Blum U, Gerig TM, Shafer SR. Mechanism by which noninhibitory concentrations of glucose increase inhibitory activity ofp-coumaric acid on morning-glory seedling biomass accumulation. J Chem Ecol. 1995 Jun;21(6):833-47. doi: 10.1007/BF02033464. PMID: 24234321.
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Phenolic acid content of soils from wheat-no till, wheat-conventional till, and fallow-conventional till soybean cropping systems.

Journal of chemical ecology

Blum U, Wentworth TR, Klein K, Worsham AD, King LD, Gerig TM, Lyu SW.
PMID: 24259167
J Chem Ecol. 1991 Jun;17(6):1045-68. doi: 10.1007/BF01402933.

Soil core (0-2.5 and/or 0-10 cm) samples were taken from wheat no till, wheat-conventional till, and fallow-conventional till soybean cropping systems from July to October of 1989 and extracted with water in an autoclave. The soil extracts were analyzed...

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Blum U, Wentworth TR, Klein K, et al. Phenolic acid content of soils from wheat-no till, wheat-conventional till, and fallow-conventional till soybean cropping systems. J Chem Ecol. 1991;17(6):1045-68doi: 10.1007/BF01402933.
Blum, U., Wentworth, T. R., Klein, K., Worsham, A. D., King, L. D., Gerig, T. M., & Lyu, S. W. (1991). Phenolic acid content of soils from wheat-no till, wheat-conventional till, and fallow-conventional till soybean cropping systems. Journal of chemical ecology, 17(6), 1045-68. https://doi.org/10.1007/BF01402933
Blum, U, et al. "Phenolic acid content of soils from wheat-no till, wheat-conventional till, and fallow-conventional till soybean cropping systems." Journal of chemical ecology vol. 17,6 (1991): 1045-68. doi: https://doi.org/10.1007/BF01402933
Blum U, Wentworth TR, Klein K, Worsham AD, King LD, Gerig TM, Lyu SW. Phenolic acid content of soils from wheat-no till, wheat-conventional till, and fallow-conventional till soybean cropping systems. J Chem Ecol. 1991 Jun;17(6):1045-68. doi: 10.1007/BF01402933. PMID: 24259167.
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Domino Tunneling.

Journal of the American Chemical Society

Schreiner PR, Wagner JP, Reisenauer HP, Gerbig D, Ley D, Sarka J, Császár AG, Vaughn A, Allen WD.
PMID: 26027801
J Am Chem Soc. 2015 Jun 24;137(24):7828-34. doi: 10.1021/jacs.5b03322. Epub 2015 Jun 15.

Matrix-isolation experiments near 3 K and state-of-the-art quantum chemical computations demonstrate that oxalic acid [1, (COOH)2] exhibits a sequential quantum mechanical tunneling phenomenon not previously observed. Intensities of numerous infrared (IR) bands were used to monitor the temporal evolution...

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Schreiner PR, Wagner JP, Reisenauer HP, et al. Domino Tunneling. J Am Chem Soc. 2015;137(24):7828-34doi: 10.1021/jacs.5b03322.
Schreiner, P. R., Wagner, J. P., Reisenauer, H. P., Gerbig, D., Ley, D., Sarka, J., Császár, A. G., Vaughn, A., & Allen, W. D. (2015). Domino Tunneling. Journal of the American Chemical Society, 137(24), 7828-34. https://doi.org/10.1021/jacs.5b03322
Schreiner, Peter R, et al. "Domino Tunneling." Journal of the American Chemical Society vol. 137,24 (2015): 7828-34. doi: https://doi.org/10.1021/jacs.5b03322
Schreiner PR, Wagner JP, Reisenauer HP, Gerbig D, Ley D, Sarka J, Császár AG, Vaughn A, Allen WD. Domino Tunneling. J Am Chem Soc. 2015 Jun 24;137(24):7828-34. doi: 10.1021/jacs.5b03322. Epub 2015 Jun 15. PMID: 26027801.
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Pre-Anthesis Reserve Utilization for Protein and Carbohydrate Synthesis in Grains of Wheat.

Plant physiology

Gebbing T, Schnyder H.
PMID: 10557235
Plant Physiol. 1999 Nov;121(3):871-878. doi: 10.1104/pp.121.3.871.

We assessed the contribution of pre-anthesis reserve C to protein and carbohydrate deposition in grains of wheat (Triticum aestivum L.) using a new approach comprised of steady-state (13)C/(12)C labeling and separation of the protein and carbohydrate fractions of mature...

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Gebbing T, Schnyder H. Pre-Anthesis Reserve Utilization for Protein and Carbohydrate Synthesis in Grains of Wheat. Plant Physiol. 1999;121(3):871-878doi: 10.1104/pp.121.3.871.
Gebbing, T., & Schnyder, H. (1999). Pre-Anthesis Reserve Utilization for Protein and Carbohydrate Synthesis in Grains of Wheat. Plant physiology, 121(3), 871-878. https://doi.org/10.1104/pp.121.3.871
Gebbing, and Schnyder. "Pre-Anthesis Reserve Utilization for Protein and Carbohydrate Synthesis in Grains of Wheat." Plant physiology vol. 121,3 (1999): 871-878. doi: https://doi.org/10.1104/pp.121.3.871
Gebbing T, Schnyder H. Pre-Anthesis Reserve Utilization for Protein and Carbohydrate Synthesis in Grains of Wheat. Plant Physiol. 1999 Nov;121(3):871-878. doi: 10.1104/pp.121.3.871. PMID: 10557235; PMCID: PMC59449.
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Aligned carbon nanotube films: production and optical and electronic properties.

Science (New York, N.Y.)

Deheer WA, Bacsa WS, Châtelain A, Gerfin T, Humphrey-Baker R, Forro L, Ugarte D.
PMID: 17792177
Science. 1995 May 12;268(5212):845-7. doi: 10.1126/science.268.5212.845.

Carbon nanotube material can now be produced in macroscopic quantities. However, the raw material has a disordered structure, which restricts investigations of both the properties and applications of the nanotubes. A method has been developed to produce thin films...

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Deheer WA, Bacsa WS, Châtelain A, et al. Aligned carbon nanotube films: production and optical and electronic properties. Science. 1995;268(5212):845-7doi: 10.1126/science.268.5212.845.
Deheer, W. A., Bacsa, W. S., Châtelain, A., Gerfin, T., Humphrey-Baker, R., Forro, L., & Ugarte, D. (1995). Aligned carbon nanotube films: production and optical and electronic properties. Science (New York, N.Y.), 268(5212), 845-7. https://doi.org/10.1126/science.268.5212.845
Deheer, W A, et al. "Aligned carbon nanotube films: production and optical and electronic properties." Science (New York, N.Y.) vol. 268,5212 (1995): 845-7. doi: https://doi.org/10.1126/science.268.5212.845
Deheer WA, Bacsa WS, Châtelain A, Gerfin T, Humphrey-Baker R, Forro L, Ugarte D. Aligned carbon nanotube films: production and optical and electronic properties. Science. 1995 May 12;268(5212):845-7. doi: 10.1126/science.268.5212.845. PMID: 17792177.
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[On the reliability of the Hirst test in diagnosis of influenza].

Zeitschrift fur die gesamte innere Medizin und ihre Grenzgebiete

BERBIG G, FRENTZEL-BEYME A.
PMID: 14901948
Z Gesamte Inn Med. 1951 Nov;6(21):645-8.

No abstract available.

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BERBIG G, FRENTZEL-BEYME A. Uber die Zuverlässigkeit des Hemmtestes nach Hirst für die Diagnose der Virusgrippe. [On the reliability of the Hirst test in diagnosis of influenza]. Z Gesamte Inn Med. 1951;6(21):645-8
BERBIG, G., & FRENTZEL-BEYME, A. (1951). Uber die Zuverlässigkeit des Hemmtestes nach Hirst für die Diagnose der Virusgrippe. [On the reliability of the Hirst test in diagnosis of influenza]. Zeitschrift fur die gesamte innere Medizin und ihre Grenzgebiete, 6(21), 645-8.
BERBIG, G, and FRENTZEL-BEYME, A. "Uber die Zuverlässigkeit des Hemmtestes nach Hirst für die Diagnose der Virusgrippe." [On the reliability of the Hirst test in diagnosis of influenza]. Zeitschrift fur die gesamte innere Medizin und ihre Grenzgebiete vol. 6,21 (1951): 645-8.
BERBIG G, FRENTZEL-BEYME A. Uber die Zuverlässigkeit des Hemmtestes nach Hirst für die Diagnose der Virusgrippe. [On the reliability of the Hirst test in diagnosis of influenza]. Z Gesamte Inn Med. 1951 Nov;6(21):645-8. Undetermined. PMID: 14901948.
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2-Chloro-6-fluoro-benzoic acid.

Acta crystallographica. Section E, Structure reports online

Betz R, Gerber T.
PMID: 21754726
Acta Crystallogr Sect E Struct Rep Online. 2011 Jun 01;67:o1329. doi: 10.1107/S1600536811016734. Epub 2011 May 07.

The title compound, C(7)H(4)ClFO(2), is a twofold halogenated derivative of benzoic acid. The C-C-C angles within the aromatic moiety cover a range 116.11 (14)-123.96 (15)°, with the maximum and the minimum value next to each other. In the crystal,...

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Betz R, Gerber T. 2-Chloro-6-fluoro-benzoic acid. Acta Crystallogr Sect E Struct Rep Online. 2011;67:o1329doi: 10.1107/S1600536811016734.
Betz, R., & Gerber, T. (2011). 2-Chloro-6-fluoro-benzoic acid. Acta crystallographica. Section E, Structure reports online, 67o1329. https://doi.org/10.1107/S1600536811016734
Betz, Richard, and Gerber, Thomas. "2-Chloro-6-fluoro-benzoic acid." Acta crystallographica. Section E, Structure reports online vol. 67 (2011): o1329. doi: https://doi.org/10.1107/S1600536811016734
Betz R, Gerber T. 2-Chloro-6-fluoro-benzoic acid. Acta Crystallogr Sect E Struct Rep Online. 2011 Jun 01;67:o1329. doi: 10.1107/S1600536811016734. Epub 2011 May 07. PMID: 21754726; PMCID: PMC3120372.
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Gain in a thallium iodide laser with external resonator.

Optics letters

Burkhard P, Gerber T, Luthy W.
PMID: 19701293
Opt Lett. 1980 Dec 01;5(12):522. doi: 10.1364/ol.5.000522.

No abstract available.

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Burkhard P, Gerber T, Luthy W. Gain in a thallium iodide laser with external resonator. Opt Lett. 1980;5(12):522doi: 10.1364/ol.5.000522.
Burkhard, P., Gerber, T., & Luthy, W. (1980). Gain in a thallium iodide laser with external resonator. Optics letters, 5(12), 522. https://doi.org/10.1364/ol.5.000522
Burkhard, P, et al. "Gain in a thallium iodide laser with external resonator." Optics letters vol. 5,12 (1980): 522. doi: https://doi.org/10.1364/ol.5.000522
Burkhard P, Gerber T, Luthy W. Gain in a thallium iodide laser with external resonator. Opt Lett. 1980 Dec 01;5(12):522. doi: 10.1364/ol.5.000522. PMID: 19701293.
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Near-infrared holography by two-photon photochemistry.

Optics letters

Gerbig V, Grygier RK, Burland DM, Sincerbox G.
PMID: 19718129
Opt Lett. 1983 Jul 01;8(7):404-6. doi: 10.1364/ol.8.000404.

The applicability of the technique of two-photon four-level photochemistry for the production of near-IR holograms is critically evaluated. Although the current best system (biacetyl in a polycyanoacrylate matrix) has low recording sensitivity, several applications of the material have been...

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Gerbig V, Grygier RK, Burland DM, et al. Near-infrared holography by two-photon photochemistry. Opt Lett. 1983;8(7):404-6doi: 10.1364/ol.8.000404.
Gerbig, V., Grygier, R. K., Burland, D. M., & Sincerbox, G. (1983). Near-infrared holography by two-photon photochemistry. Optics letters, 8(7), 404-6. https://doi.org/10.1364/ol.8.000404
Gerbig, V, et al. "Near-infrared holography by two-photon photochemistry." Optics letters vol. 8,7 (1983): 404-6. doi: https://doi.org/10.1364/ol.8.000404
Gerbig V, Grygier RK, Burland DM, Sincerbox G. Near-infrared holography by two-photon photochemistry. Opt Lett. 1983 Jul 01;8(7):404-6. doi: 10.1364/ol.8.000404. PMID: 19718129.
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Photoionization of three isomers of the C9H7 radical.

The journal of physical chemistry. A

Hemberger P, Steinbauer M, Schneider M, Fischer I, Johnson M, Bodi A, Gerber T.
PMID: 19813740
J Phys Chem A. 2010 Apr 15;114(14):4698-703. doi: 10.1021/jp9068569.

Three resonance-stabilized radicals, 1-indenyl (Ind), 1-phenylpropargyl (1PPR), and 3-phenylpropargyl (3PPR), all isomers of the composition C(9)H(7), were generated by jet flash pyrolysis. Their photoionization was examined by VUV synchrotron radiation. The mass spectra show a clean and efficient radical...

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Hemberger P, Steinbauer M, Schneider M, et al. Photoionization of three isomers of the C9H7 radical. J Phys Chem A. 2010;114(14):4698-703doi: 10.1021/jp9068569.
Hemberger, P., Steinbauer, M., Schneider, M., Fischer, I., Johnson, M., Bodi, A., & Gerber, T. (2010). Photoionization of three isomers of the C9H7 radical. The journal of physical chemistry. A, 114(14), 4698-703. https://doi.org/10.1021/jp9068569
Hemberger, Patrick, et al. "Photoionization of three isomers of the C9H7 radical." The journal of physical chemistry. A vol. 114,14 (2010): 4698-703. doi: https://doi.org/10.1021/jp9068569
Hemberger P, Steinbauer M, Schneider M, Fischer I, Johnson M, Bodi A, Gerber T. Photoionization of three isomers of the C9H7 radical. J Phys Chem A. 2010 Apr 15;114(14):4698-703. doi: 10.1021/jp9068569. PMID: 19813740.
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"Hot standards" for the thermoacidophilic archaeon Sulfolobus solfataricus.

Extremophiles : life under extreme conditions

Zaparty M, Esser D, Gertig S, Haferkamp P, Kouril T, Manica A, Pham TK, Reimann J, Schreiber K, Sierocinski P, Teichmann D, van Wolferen M, von Jan M, Wieloch P, Albers SV, Driessen AJ, Klenk HP, Schleper C, Schomburg D, van der Oost J, Wright PC, Siebers B.
PMID: 19802714
Extremophiles. 2010 Jan;14(1):119-42. doi: 10.1007/s00792-009-0280-0. Epub 2009 Oct 04.

Within the archaea, the thermoacidophilic crenarchaeote Sulfolobus solfataricus has become an important model organism for physiology and biochemistry, comparative and functional genomics, as well as, more recently also for systems biology approaches. Within the Sulfolobus Systems Biology ("SulfoSYS")-project the...

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Zaparty M, Esser D, Gertig S, et al. "Hot standards" for the thermoacidophilic archaeon Sulfolobus solfataricus. Extremophiles. 2009;14(1):119-42doi: 10.1007/s00792-009-0280-0.
Zaparty, M., Esser, D., Gertig, S., Haferkamp, P., Kouril, T., Manica, A., Pham, T. K., Reimann, J., Schreiber, K., Sierocinski, P., Teichmann, D., van Wolferen, M., von Jan, M., Wieloch, P., Albers, S. V., Driessen, A. J., Klenk, H. P., Schleper, C., Schomburg, D., van der Oost, J., Wright, P. C., & Siebers, B. (2010). "Hot standards" for the thermoacidophilic archaeon Sulfolobus solfataricus. Extremophiles : life under extreme conditions, 14(1), 119-42. https://doi.org/10.1007/s00792-009-0280-0
Zaparty, Melanie, et al. ""Hot standards" for the thermoacidophilic archaeon Sulfolobus solfataricus." Extremophiles : life under extreme conditions vol. 14,1 (2010): 119-42. doi: https://doi.org/10.1007/s00792-009-0280-0
Zaparty M, Esser D, Gertig S, Haferkamp P, Kouril T, Manica A, Pham TK, Reimann J, Schreiber K, Sierocinski P, Teichmann D, van Wolferen M, von Jan M, Wieloch P, Albers SV, Driessen AJ, Klenk HP, Schleper C, Schomburg D, van der Oost J, Wright PC, Siebers B. "Hot standards" for the thermoacidophilic archaeon Sulfolobus solfataricus. Extremophiles. 2010 Jan;14(1):119-42. doi: 10.1007/s00792-009-0280-0. Epub 2009 Oct 04. PMID: 19802714; PMCID: PMC2797409.
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Showing 1 to 12 of 265 entries