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π-Conjugated [2]Catenanes Based on Oligothiophenes and Phenanthrolines: Efficient Synthesis and Electronic Properties.

Chemistry (Weinheim an der Bergstrasse, Germany)

Götz G, Zhu X, Mishra A, Segura JL, Mena-Osteritz E, Bäuerle P.
PMID: 25820180
Chemistry. 2015 May 04;21(19):7193-210. doi: 10.1002/chem.201406039. Epub 2015 Mar 25.

Novel π-conjugated topologies based on oligothiophenes and phenanthroline have been assembled by combining their outstanding electronic and structural benefits with the specific properties of the topological structure. Macrocycles and catenanes are prepared by using an optimized protocol of transition...

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Götz G, Zhu X, Mishra A, et al. π-Conjugated [2]Catenanes Based on Oligothiophenes and Phenanthrolines: Efficient Synthesis and Electronic Properties. Chemistry. 2015;21(19):7193-210doi: 10.1002/chem.201406039.
Götz, G., Zhu, X., Mishra, A., Segura, J. L., Mena-Osteritz, E., & Bäuerle, P. (2015). π-Conjugated [2]Catenanes Based on Oligothiophenes and Phenanthrolines: Efficient Synthesis and Electronic Properties. Chemistry (Weinheim an der Bergstrasse, Germany), 21(19), 7193-210. https://doi.org/10.1002/chem.201406039
Götz, Günther, et al. "π-Conjugated [2]Catenanes Based on Oligothiophenes and Phenanthrolines: Efficient Synthesis and Electronic Properties." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,19 (2015): 7193-210. doi: https://doi.org/10.1002/chem.201406039
Götz G, Zhu X, Mishra A, Segura JL, Mena-Osteritz E, Bäuerle P. π-Conjugated [2]Catenanes Based on Oligothiophenes and Phenanthrolines: Efficient Synthesis and Electronic Properties. Chemistry. 2015 May 04;21(19):7193-210. doi: 10.1002/chem.201406039. Epub 2015 Mar 25. PMID: 25820180.
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Reaction of Organolithium Reagents with Tetracarbonyl[2-(phenyl-kappaC(2')),pyridine-kappaN]rhenium(I): Isolation and Structural Characterization of Acyl Rhenate Species.

Inorganic chemistry

Djukic JP, Dötz KH, Pfeffer M, De Cian A, Fischer J.
PMID: 11670459
Inorg Chem. 1998 Jul 13;37(14):3649-3651. doi: 10.1021/ic980016e.

No abstract available.

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Djukic JP, Dötz KH, Pfeffer M, et al. Reaction of Organolithium Reagents with Tetracarbonyl[2-(phenyl-kappaC(2')),pyridine-kappaN]rhenium(I): Isolation and Structural Characterization of Acyl Rhenate Species. Inorg Chem. 1998;37(14):3649-3651doi: 10.1021/ic980016e.
Djukic, J. P., Dötz, K. H., Pfeffer, M., De Cian, A., & Fischer, J. (1998). Reaction of Organolithium Reagents with Tetracarbonyl[2-(phenyl-kappaC(2')),pyridine-kappaN]rhenium(I): Isolation and Structural Characterization of Acyl Rhenate Species. Inorganic chemistry, 37(14), 3649-3651. https://doi.org/10.1021/ic980016e
Djukic, Jean-Pierre, et al. "Reaction of Organolithium Reagents with Tetracarbonyl[2-(phenyl-kappaC(2')),pyridine-kappaN]rhenium(I): Isolation and Structural Characterization of Acyl Rhenate Species." Inorganic chemistry vol. 37,14 (1998): 3649-3651. doi: https://doi.org/10.1021/ic980016e
Djukic JP, Dötz KH, Pfeffer M, De Cian A, Fischer J. Reaction of Organolithium Reagents with Tetracarbonyl[2-(phenyl-kappaC(2')),pyridine-kappaN]rhenium(I): Isolation and Structural Characterization of Acyl Rhenate Species. Inorg Chem. 1998 Jul 13;37(14):3649-3651. doi: 10.1021/ic980016e. PMID: 11670459.
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[Report of the 34th meeting of the Swiss Dermatological Society].

Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete

GOTZ H.
PMID: 13068757
Hautarzt. 1953 Feb;4(2):84.

No abstract available.

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GOTZ H. Bericht über die 34. Jahrestagung der Schweizerischen Dermatologischen Gesellschaft. [Report of the 34th meeting of the Swiss Dermatological Society]. Hautarzt. 1953;4(2):84
GOTZ, H. (1953). Bericht über die 34. Jahrestagung der Schweizerischen Dermatologischen Gesellschaft. [Report of the 34th meeting of the Swiss Dermatological Society]. Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 4(2), 84.
GOTZ, H. "Bericht über die 34. Jahrestagung der Schweizerischen Dermatologischen Gesellschaft." [Report of the 34th meeting of the Swiss Dermatological Society]. Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete vol. 4,2 (1953): 84.
GOTZ H. Bericht über die 34. Jahrestagung der Schweizerischen Dermatologischen Gesellschaft. [Report of the 34th meeting of the Swiss Dermatological Society]. Hautarzt. 1953 Feb;4(2):84. Undetermined. PMID: 13068757.
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A metal-carbene carbohydrate amphiphile as a low-molecular-mass organometallic gelator.

Angewandte Chemie (International ed. in English)

Bühler G, Feiters MC, Nolte RJ, Dötz KH.
PMID: 12800168
Angew Chem Int Ed Engl. 2003 Jun 06;42(22):2494-7. doi: 10.1002/anie.200351134.

No abstract available.

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Bühler G, Feiters MC, Nolte RJ, et al. A metal-carbene carbohydrate amphiphile as a low-molecular-mass organometallic gelator. Angew Chem Int Ed Engl. 2003;42(22):2494-7doi: 10.1002/anie.200351134.
Bühler, G., Feiters, M. C., Nolte, R. J., & Dötz, K. H. (2003). A metal-carbene carbohydrate amphiphile as a low-molecular-mass organometallic gelator. Angewandte Chemie (International ed. in English), 42(22), 2494-7. https://doi.org/10.1002/anie.200351134
Bühler, Gunnar, et al. "A metal-carbene carbohydrate amphiphile as a low-molecular-mass organometallic gelator." Angewandte Chemie (International ed. in English) vol. 42,22 (2003): 2494-7. doi: https://doi.org/10.1002/anie.200351134
Bühler G, Feiters MC, Nolte RJ, Dötz KH. A metal-carbene carbohydrate amphiphile as a low-molecular-mass organometallic gelator. Angew Chem Int Ed Engl. 2003 Jun 06;42(22):2494-7. doi: 10.1002/anie.200351134. PMID: 12800168.
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Some structural requirements for the antibiotic action of distamycins.

FEBS letters

Chandra P, Götz A, Wacker A, Verini MA, Casazza AM, Fioretti A, Arcamone F, Ghione M.
PMID: 11945953
FEBS Lett. 1971 Sep 01;16(4):249-252. doi: 10.1016/0014-5793(71)80362-9.

No abstract available.

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Chandra P, Götz A, Wacker A, et al. Some structural requirements for the antibiotic action of distamycins. FEBS Lett. 1971;16(4):249-252doi: 10.1016/0014-5793(71)80362-9.
Chandra, P., Götz, A., Wacker, A., Verini, M. A., Casazza, A. M., Fioretti, A., Arcamone, F., & Ghione, M. (1971). Some structural requirements for the antibiotic action of distamycins. FEBS letters, 16(4), 249-252. https://doi.org/10.1016/0014-5793(71)80362-9
Chandra, P, et al. "Some structural requirements for the antibiotic action of distamycins." FEBS letters vol. 16,4 (1971): 249-252. doi: https://doi.org/10.1016/0014-5793(71)80362-9
Chandra P, Götz A, Wacker A, Verini MA, Casazza AM, Fioretti A, Arcamone F, Ghione M. Some structural requirements for the antibiotic action of distamycins. FEBS Lett. 1971 Sep 01;16(4):249-252. doi: 10.1016/0014-5793(71)80362-9. PMID: 11945953.
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[On the clinical aspects of hypertension].

Das Deutsche Gesundheitswesen

DUTZ H.
PMID: 13818923
Dtsch Gesundheitsw. 1959 Jul 23;14:1369-73.

No abstract available.

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DUTZ H. [On the clinical aspects of hypertension]. Dtsch Gesundheitsw. 1959;14:1369-73
DUTZ, H. (1959). [On the clinical aspects of hypertension]. Das Deutsche Gesundheitswesen, 141369-73.
DUTZ, H. "[On the clinical aspects of hypertension]." Das Deutsche Gesundheitswesen vol. 14 (1959): 1369-73.
DUTZ H. [On the clinical aspects of hypertension]. Dtsch Gesundheitsw. 1959 Jul 23;14:1369-73. German. PMID: 13818923.
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Efficient air-stable organometallic low-molecular-mass gelators for ionic liquids: synthesis, aggregation and application of pyridine-bridged bis(benzimidazolylidene)-palladium complexes.

Chemistry (Weinheim an der Bergstrasse, Germany)

Tu T, Bao X, Assenmacher W, Peterlik H, Daniels J, Dötz KH.
PMID: 19123219
Chemistry. 2009;15(8):1853-61. doi: 10.1002/chem.200802116.

Novel pincer-type, pyridine-bridged bis(benzimidazolylidene)-palladium complexes 5-7 were synthesised from cheap commercial precursors under microwave assistance. Although simple in structure, carbene complexes 5a,b are efficient low-molecular-mass metallogelators. They gelate not only a broad variety of protic and aprotic organic solvents,...

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Tu T, Bao X, Assenmacher W, et al. Efficient air-stable organometallic low-molecular-mass gelators for ionic liquids: synthesis, aggregation and application of pyridine-bridged bis(benzimidazolylidene)-palladium complexes. Chemistry. 2009;15(8):1853-61doi: 10.1002/chem.200802116.
Tu, T., Bao, X., Assenmacher, W., Peterlik, H., Daniels, J., & Dötz, K. H. (2009). Efficient air-stable organometallic low-molecular-mass gelators for ionic liquids: synthesis, aggregation and application of pyridine-bridged bis(benzimidazolylidene)-palladium complexes. Chemistry (Weinheim an der Bergstrasse, Germany), 15(8), 1853-61. https://doi.org/10.1002/chem.200802116
Tu, Tao, et al. "Efficient air-stable organometallic low-molecular-mass gelators for ionic liquids: synthesis, aggregation and application of pyridine-bridged bis(benzimidazolylidene)-palladium complexes." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 15,8 (2009): 1853-61. doi: https://doi.org/10.1002/chem.200802116
Tu T, Bao X, Assenmacher W, Peterlik H, Daniels J, Dötz KH. Efficient air-stable organometallic low-molecular-mass gelators for ionic liquids: synthesis, aggregation and application of pyridine-bridged bis(benzimidazolylidene)-palladium complexes. Chemistry. 2009;15(8):1853-61. doi: 10.1002/chem.200802116. PMID: 19123219.
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"Double-concave" graphene: permethoxylated hexa-peri-hexabenzocoronene and its cocrystals with hexafluorobenzene and fullerene.

Angewandte Chemie (International ed. in English)

Wang Z, Dötz F, Enkelmann V, Müllen K.
PMID: 15565664
Angew Chem Int Ed Engl. 2005 Feb 11;44(8):1247-50. doi: 10.1002/anie.200461445.

No abstract available.

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Wang Z, Dötz F, Enkelmann V, et al. "Double-concave" graphene: permethoxylated hexa-peri-hexabenzocoronene and its cocrystals with hexafluorobenzene and fullerene. Angew Chem Int Ed Engl. 2005;44(8):1247-50doi: 10.1002/anie.200461445.
Wang, Z., Dötz, F., Enkelmann, V., & Müllen, K. (2005). "Double-concave" graphene: permethoxylated hexa-peri-hexabenzocoronene and its cocrystals with hexafluorobenzene and fullerene. Angewandte Chemie (International ed. in English), 44(8), 1247-50. https://doi.org/10.1002/anie.200461445
Wang, Zhaohui, et al. ""Double-concave" graphene: permethoxylated hexa-peri-hexabenzocoronene and its cocrystals with hexafluorobenzene and fullerene." Angewandte Chemie (International ed. in English) vol. 44,8 (2005): 1247-50. doi: https://doi.org/10.1002/anie.200461445
Wang Z, Dötz F, Enkelmann V, Müllen K. "Double-concave" graphene: permethoxylated hexa-peri-hexabenzocoronene and its cocrystals with hexafluorobenzene and fullerene. Angew Chem Int Ed Engl. 2005 Feb 11;44(8):1247-50. doi: 10.1002/anie.200461445. PMID: 15565664.
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Normal vector method for the RCWA with automated vector field generation.

Optics express

Götz P, Schuster T, Frenner K, Rafler S, Osten W.
PMID: 18958012
Opt Express. 2008 Oct 27;16(22):17295-301. doi: 10.1364/oe.16.017295.

Early formulations of the RCWA yield, implicated by the erroneous application of factorization rules to discrete Fourier transformations, poor convergence in certain cases. An explanation for this finding and an approach to overcome the problem for crossed gratings was...

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Götz P, Schuster T, Frenner K, et al. Normal vector method for the RCWA with automated vector field generation. Opt Express. 2008;16(22):17295-301doi: 10.1364/oe.16.017295.
Götz, P., Schuster, T., Frenner, K., Rafler, S., & Osten, W. (2008). Normal vector method for the RCWA with automated vector field generation. Optics express, 16(22), 17295-301. https://doi.org/10.1364/oe.16.017295
Götz, Peter, et al. "Normal vector method for the RCWA with automated vector field generation." Optics express vol. 16,22 (2008): 17295-301. doi: https://doi.org/10.1364/oe.16.017295
Götz P, Schuster T, Frenner K, Rafler S, Osten W. Normal vector method for the RCWA with automated vector field generation. Opt Express. 2008 Oct 27;16(22):17295-301. doi: 10.1364/oe.16.017295. PMID: 18958012.
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Apoptotic morphology does not always require caspase activity in rat cerebellar granule neurons.

Neurotoxicity research

Daré E, Gorman AM, Ahlbom E, Götz M, Momoi T, Ceccatelli S.
PMID: 14715461
Neurotox Res. 2001 Oct;3(5):501-14. doi: 10.1007/BF03033206.

The death of a cell via apoptosis is characterized by morphological changes including cell shrinkage and nuclear condensation. Intracellularly, proteases, including caspases, are activated. In the present article we have compared the ability of three different neurotoxic agents to...

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Daré E, Gorman AM, Ahlbom E, et al. Apoptotic morphology does not always require caspase activity in rat cerebellar granule neurons. Neurotox Res. 2001;3(5):501-14doi: 10.1007/BF03033206.
Daré, E., Gorman, A. M., Ahlbom, E., Götz, M., Momoi, T., & Ceccatelli, S. (2001). Apoptotic morphology does not always require caspase activity in rat cerebellar granule neurons. Neurotoxicity research, 3(5), 501-14. https://doi.org/10.1007/BF03033206
Daré, E, et al. "Apoptotic morphology does not always require caspase activity in rat cerebellar granule neurons." Neurotoxicity research vol. 3,5 (2001): 501-14. doi: https://doi.org/10.1007/BF03033206
Daré E, Gorman AM, Ahlbom E, Götz M, Momoi T, Ceccatelli S. Apoptotic morphology does not always require caspase activity in rat cerebellar granule neurons. Neurotox Res. 2001 Oct;3(5):501-14. doi: 10.1007/BF03033206. PMID: 14715461.
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Oligothiophene-based catenanes: synthesis and electronic properties of a novel conjugated topological structure.

Angewandte Chemie (International ed. in English)

Bäuerle P, Ammann M, Wilde M, Götz G, Mena-Osteritz E, Rang A, Schalley CA.
PMID: 17075935
Angew Chem Int Ed Engl. 2007;46(3):363-8. doi: 10.1002/anie.200602652.

No abstract available.

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Bäuerle P, Ammann M, Wilde M, et al. Oligothiophene-based catenanes: synthesis and electronic properties of a novel conjugated topological structure. Angew Chem Int Ed Engl. 2007;46(3):363-8doi: 10.1002/anie.200602652.
Bäuerle, P., Ammann, M., Wilde, M., Götz, G., Mena-Osteritz, E., Rang, A., & Schalley, C. A. (2007). Oligothiophene-based catenanes: synthesis and electronic properties of a novel conjugated topological structure. Angewandte Chemie (International ed. in English), 46(3), 363-8. https://doi.org/10.1002/anie.200602652
Bäuerle, Peter, et al. "Oligothiophene-based catenanes: synthesis and electronic properties of a novel conjugated topological structure." Angewandte Chemie (International ed. in English) vol. 46,3 (2007): 363-8. doi: https://doi.org/10.1002/anie.200602652
Bäuerle P, Ammann M, Wilde M, Götz G, Mena-Osteritz E, Rang A, Schalley CA. Oligothiophene-based catenanes: synthesis and electronic properties of a novel conjugated topological structure. Angew Chem Int Ed Engl. 2007;46(3):363-8. doi: 10.1002/anie.200602652. PMID: 17075935.
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An update on the toxicity of Abeta in Alzheimer's disease.

Neuropsychiatric disease and treatment

Götz J, Ittner LM, Schonrock N, Cappai R.
PMID: 19337449
Neuropsychiatr Dis Treat. 2008 Dec;4(6):1033-42. doi: 10.2147/ndt.s3016.

Alzheimer's disease is characterized histopathologically by deposition of insoluble forms of the peptide Abeta and the protein tau in brain. Abeta is the principal component of amyloid plaques and tau of neurofibrillary tangles. Familial cases of AD are associated...

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Götz J, Ittner LM, Schonrock N, et al. An update on the toxicity of Abeta in Alzheimer's disease. Neuropsychiatr Dis Treat. 2008;4(6):1033-42doi: 10.2147/ndt.s3016.
Götz, J., Ittner, L. M., Schonrock, N., & Cappai, R. (2008). An update on the toxicity of Abeta in Alzheimer's disease. Neuropsychiatric disease and treatment, 4(6), 1033-42. https://doi.org/10.2147/ndt.s3016
Götz, Jürgen, et al. "An update on the toxicity of Abeta in Alzheimer's disease." Neuropsychiatric disease and treatment vol. 4,6 (2008): 1033-42. doi: https://doi.org/10.2147/ndt.s3016
Götz J, Ittner LM, Schonrock N, Cappai R. An update on the toxicity of Abeta in Alzheimer's disease. Neuropsychiatr Dis Treat. 2008 Dec;4(6):1033-42. doi: 10.2147/ndt.s3016. PMID: 19337449; PMCID: PMC2646638.
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Showing 13 to 24 of 503 entries