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Developing key competencies for sustainable development in higher education

informal education

Barth M, Godemann J, Rieckmann M.
GSID: n3PsYP84LtQJ
M Barth, J Godemann, M Rieckmann… - … in higher education, 2007 - emerald.com

… consider, the possibilities both of formal and informal learning and their relationship to competence development within higher education. … Characteristics of learning in informal settings Informal learning has to be distinguished from formal and informal education. It does...

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Barth, M., Godemann, J., Rieckmann, M., & Stoltenberg, U. (2007). Developing key competencies for sustainable development in higher education. International Journal of sustainability in higher education.
Barth, Matthias, et al. "Developing key competencies for sustainable development in higher education." International Journal of sustainability in higher education (2007).
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Irreversible inhibitors of the 3C protease of Coxsackie virus through templated assembly of protein-binding fragments.

Nature communications

Becker D, Kaczmarska Z, Arkona C, Schulz R, Tauber C, Wolber G, Hilgenfeld R, Coll M, Rademann J.
PMID: 27677239
Nat Commun. 2016 Sep 28;7:12761. doi: 10.1038/ncomms12761.

Small-molecule fragments binding to biomacromolecules can be starting points for the development of drugs, but are often difficult to detect due to low affinities. Here we present a strategy that identifies protein-binding fragments through their potential to induce the...

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Becker D, Kaczmarska Z, Arkona C, et al. Irreversible inhibitors of the 3C protease of Coxsackie virus through templated assembly of protein-binding fragments. Nat Commun. 2016;7:12761doi: 10.1038/ncomms12761.
Becker, D., Kaczmarska, Z., Arkona, C., Schulz, R., Tauber, C., Wolber, G., Hilgenfeld, R., Coll, M., & Rademann, J. (2016). Irreversible inhibitors of the 3C protease of Coxsackie virus through templated assembly of protein-binding fragments. Nature communications, 712761. https://doi.org/10.1038/ncomms12761
Becker, Daniel, et al. "Irreversible inhibitors of the 3C protease of Coxsackie virus through templated assembly of protein-binding fragments." Nature communications vol. 7 (2016): 12761. doi: https://doi.org/10.1038/ncomms12761
Becker D, Kaczmarska Z, Arkona C, Schulz R, Tauber C, Wolber G, Hilgenfeld R, Coll M, Rademann J. Irreversible inhibitors of the 3C protease of Coxsackie virus through templated assembly of protein-binding fragments. Nat Commun. 2016 Sep 28;7:12761. doi: 10.1038/ncomms12761. PMID: 27677239; PMCID: PMC5052702.
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Crystal structure of 1-hy-droxy-2,2,6,6-tetra-methyl-piperidin-1-ium tri-fluoro-methane-sulfonate.

Acta crystallographica. Section E, Crystallographic communications

Godemann C, Spannenberg A, Beweries T.
PMID: 26870528
Acta Crystallogr E Crystallogr Commun. 2015 Nov 07;71:o921. doi: 10.1107/S2056989015020897. eCollection 2015 Dec 01.

In the cation of the title salt, C9H20NO(+)·CF3O3S(-), the six-membered heterocyclic ring displays a chair conformation. In the crystal, centrosymmetric pairs of cations and anions are linked by N-H⋯O and O-H⋯O hydrogen bonds to form rings with a R...

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Godemann C, Spannenberg A, Beweries T. Crystal structure of 1-hy-droxy-2,2,6,6-tetra-methyl-piperidin-1-ium tri-fluoro-methane-sulfonate. Acta Crystallogr E Crystallogr Commun. 2015;71:o921doi: 10.1107/S2056989015020897.
Godemann, C., Spannenberg, A., & Beweries, T. (2015). Crystal structure of 1-hy-droxy-2,2,6,6-tetra-methyl-piperidin-1-ium tri-fluoro-methane-sulfonate. Acta crystallographica. Section E, Crystallographic communications, 71o921. https://doi.org/10.1107/S2056989015020897
Godemann, Christian, et al. "Crystal structure of 1-hy-droxy-2,2,6,6-tetra-methyl-piperidin-1-ium tri-fluoro-methane-sulfonate." Acta crystallographica. Section E, Crystallographic communications vol. 71 (2015): o921. doi: https://doi.org/10.1107/S2056989015020897
Godemann C, Spannenberg A, Beweries T. Crystal structure of 1-hy-droxy-2,2,6,6-tetra-methyl-piperidin-1-ium tri-fluoro-methane-sulfonate. Acta Crystallogr E Crystallogr Commun. 2015 Nov 07;71:o921. doi: 10.1107/S2056989015020897. eCollection 2015 Dec 01. PMID: 26870528; PMCID: PMC4719881.
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Mechanochemically Induced Conversion of Crystalline Benzamide Polymorphs by Seeding.

Angewandte Chemie (International ed. in English)

Fischer F, Greiser S, Pfeifer D, Jäger C, Rademann K, Emmerling F.
PMID: 27763713
Angew Chem Int Ed Engl. 2016 Nov 07;55(46):14281-14285. doi: 10.1002/anie.201607358. Epub 2016 Oct 20.

Benzamide has been known for its polymorphism for almost 200 years. Three polymorphic forms are described. To date, it was only possible to crystallize a metastable form in a mixture together with the thermodynamically most stable form I. A...

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Fischer F, Greiser S, Pfeifer D, et al. Mechanochemically Induced Conversion of Crystalline Benzamide Polymorphs by Seeding. Angew Chem Int Ed Engl. 2016;55(46):14281-14285doi: 10.1002/anie.201607358.
Fischer, F., Greiser, S., Pfeifer, D., Jäger, C., Rademann, K., & Emmerling, F. (2016). Mechanochemically Induced Conversion of Crystalline Benzamide Polymorphs by Seeding. Angewandte Chemie (International ed. in English), 55(46), 14281-14285. https://doi.org/10.1002/anie.201607358
Fischer, Franziska, et al. "Mechanochemically Induced Conversion of Crystalline Benzamide Polymorphs by Seeding." Angewandte Chemie (International ed. in English) vol. 55,46 (2016): 14281-14285. doi: https://doi.org/10.1002/anie.201607358
Fischer F, Greiser S, Pfeifer D, Jäger C, Rademann K, Emmerling F. Mechanochemically Induced Conversion of Crystalline Benzamide Polymorphs by Seeding. Angew Chem Int Ed Engl. 2016 Nov 07;55(46):14281-14285. doi: 10.1002/anie.201607358. Epub 2016 Oct 20. PMID: 27763713.
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Crystal structure of 1,1,2,2-tetra-methyl-1,2-bis-(2,3,4,5-tetra-methyl-cyclo-penta-2,4-dien-1-yl)disilane.

Acta crystallographica. Section E, Crystallographic communications

Godemann C, Spannenberg A, Beweries T.
PMID: 26594581
Acta Crystallogr E Crystallogr Commun. 2015 Oct 28;71:o888. doi: 10.1107/S2056989015019891. eCollection 2015 Nov 01.

The mol-ecular structure of the title compound, C22H38Si2, features a trans arrangement of the cyclo-penta-dienyl rings to avoid steric strain [C-Si-Si-C torsion angle = -179.0 (5)°]. The Si-Si bond length is 2.3444 (4) Å. The most notable inter-molecular inter-actions...

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Godemann C, Spannenberg A, Beweries T. Crystal structure of 1,1,2,2-tetra-methyl-1,2-bis-(2,3,4,5-tetra-methyl-cyclo-penta-2,4-dien-1-yl)disilane. Acta Crystallogr E Crystallogr Commun. 2015;71:o888doi: 10.1107/S2056989015019891.
Godemann, C., Spannenberg, A., & Beweries, T. (2015). Crystal structure of 1,1,2,2-tetra-methyl-1,2-bis-(2,3,4,5-tetra-methyl-cyclo-penta-2,4-dien-1-yl)disilane. Acta crystallographica. Section E, Crystallographic communications, 71o888. https://doi.org/10.1107/S2056989015019891
Godemann, Christian, et al. "Crystal structure of 1,1,2,2-tetra-methyl-1,2-bis-(2,3,4,5-tetra-methyl-cyclo-penta-2,4-dien-1-yl)disilane." Acta crystallographica. Section E, Crystallographic communications vol. 71 (2015): o888. doi: https://doi.org/10.1107/S2056989015019891
Godemann C, Spannenberg A, Beweries T. Crystal structure of 1,1,2,2-tetra-methyl-1,2-bis-(2,3,4,5-tetra-methyl-cyclo-penta-2,4-dien-1-yl)disilane. Acta Crystallogr E Crystallogr Commun. 2015 Oct 28;71:o888. doi: 10.1107/S2056989015019891. eCollection 2015 Nov 01. PMID: 26594581; PMCID: PMC4644997.
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Completing the picture for the smallest eigenvalue of real Wishart matrices.

Physical review letters

Akemann G, Guhr T, Kieburg M, Wegner R, Wirtz T.
PMID: 25554862
Phys Rev Lett. 2014 Dec 19;113(25):250201. doi: 10.1103/PhysRevLett.113.250201. Epub 2014 Dec 19.

Rectangular real N×(N+ν) matrices W with a Gaussian distribution appear very frequently in data analysis, condensed matter physics, and quantum field theory. A central question concerns the correlations encoded in the spectral statistics of WW^{T}. The extreme eigenvalues of...

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Akemann G, Guhr T, Kieburg M, et al. Completing the picture for the smallest eigenvalue of real Wishart matrices. Phys Rev Lett. 2014;113(25):250201doi: 10.1103/PhysRevLett.113.250201.
Akemann, G., Guhr, T., Kieburg, M., Wegner, R., & Wirtz, T. (2014). Completing the picture for the smallest eigenvalue of real Wishart matrices. Physical review letters, 113(25), 250201. https://doi.org/10.1103/PhysRevLett.113.250201
Akemann, G, et al. "Completing the picture for the smallest eigenvalue of real Wishart matrices." Physical review letters vol. 113,25 (2014): 250201. doi: https://doi.org/10.1103/PhysRevLett.113.250201
Akemann G, Guhr T, Kieburg M, Wegner R, Wirtz T. Completing the picture for the smallest eigenvalue of real Wishart matrices. Phys Rev Lett. 2014 Dec 19;113(25):250201. doi: 10.1103/PhysRevLett.113.250201. Epub 2014 Dec 19. PMID: 25554862.
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Interaction of dermatologically relevant nanoparticles with skin cells and skin.

Beilstein journal of nanotechnology

Vogt A, Rancan F, Ahlberg S, Nazemi B, Choe CS, Darvin ME, Hadam S, Blume-Peytavi U, Loza K, Diendorf J, Epple M, Graf C, Rühl E, Meinke MC, Lademann J.
PMID: 25551064
Beilstein J Nanotechnol. 2014 Dec 08;5:2363-73. doi: 10.3762/bjnano.5.245. eCollection 2014.

The investigation of nanoparticle interactions with tissues is complex. High levels of standardization, ideally testing of different material types in the same biological model, and combinations of sensitive imaging and detection methods are required. Here, we present our studies...

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Vogt A, Rancan F, Ahlberg S, et al. Interaction of dermatologically relevant nanoparticles with skin cells and skin. Beilstein J Nanotechnol. 2014;5:2363-73doi: 10.3762/bjnano.5.245.
Vogt, A., Rancan, F., Ahlberg, S., Nazemi, B., Choe, C. S., Darvin, M. E., Hadam, S., Blume-Peytavi, U., Loza, K., Diendorf, J., Epple, M., Graf, C., Rühl, E., Meinke, M. C., & Lademann, J. (2014). Interaction of dermatologically relevant nanoparticles with skin cells and skin. Beilstein journal of nanotechnology, 52363-73. https://doi.org/10.3762/bjnano.5.245
Vogt, Annika, et al. "Interaction of dermatologically relevant nanoparticles with skin cells and skin." Beilstein journal of nanotechnology vol. 5 (2014): 2363-73. doi: https://doi.org/10.3762/bjnano.5.245
Vogt A, Rancan F, Ahlberg S, Nazemi B, Choe CS, Darvin ME, Hadam S, Blume-Peytavi U, Loza K, Diendorf J, Epple M, Graf C, Rühl E, Meinke MC, Lademann J. Interaction of dermatologically relevant nanoparticles with skin cells and skin. Beilstein J Nanotechnol. 2014 Dec 08;5:2363-73. doi: 10.3762/bjnano.5.245. eCollection 2014. PMID: 25551064; PMCID: PMC4273260.
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Fibrous Pseudotumor of the Tunica Vaginalis of the Scrotum: Is there a Typical Ultrasound Pattern?.

Ultrasound international open

Ohana M, Lindner V, Labani A, Alemann G, Lang H, Roy C.
PMID: 27689166
Ultrasound Int Open. 2016 Mar;2(1):E34-6. doi: 10.1055/s-0035-1569412.

No abstract available.

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Ohana M, Lindner V, Labani A, et al. Fibrous Pseudotumor of the Tunica Vaginalis of the Scrotum: Is there a Typical Ultrasound Pattern?. Ultrasound Int Open. 2016;2(1):E34-6doi: 10.1055/s-0035-1569412.
Ohana, M., Lindner, V., Labani, A., Alemann, G., Lang, H., & Roy, C. (2016). Fibrous Pseudotumor of the Tunica Vaginalis of the Scrotum: Is there a Typical Ultrasound Pattern?. Ultrasound international open, 2(1), E34-6. https://doi.org/10.1055/s-0035-1569412
Ohana, M, et al. "Fibrous Pseudotumor of the Tunica Vaginalis of the Scrotum: Is there a Typical Ultrasound Pattern?." Ultrasound international open vol. 2,1 (2016): E34-6. doi: https://doi.org/10.1055/s-0035-1569412
Ohana M, Lindner V, Labani A, Alemann G, Lang H, Roy C. Fibrous Pseudotumor of the Tunica Vaginalis of the Scrotum: Is there a Typical Ultrasound Pattern?. Ultrasound Int Open. 2016 Mar;2(1):E34-6. doi: 10.1055/s-0035-1569412. PMID: 27689166; PMCID: PMC5023218.
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Control of CO2 fixation regulation of stromal fructose-1,6-bisphosphatase in spinach by pH and Mg(2+) concentration.

Planta

Gardemann A, Schimkat D, Heldt HW.
PMID: 24232331
Planta. 1986 Sep;168(4):536-45. doi: 10.1007/BF00392274.

The effect of pH and of Mg(2+) concentration on the light activated form of stromal fructose-1,6-bisphosphatase (FBPase) was studied using the enzyme rapidly extracted from illuminated spinach chloroplasts. The (fructose-1,6-bisphosphate(4-))(Mg(2+)) complex has been identified as the substrate of the...

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Gardemann A, Schimkat D, Heldt HW. Control of CO2 fixation regulation of stromal fructose-1,6-bisphosphatase in spinach by pH and Mg(2+) concentration. Planta. 1986;168(4):536-45doi: 10.1007/BF00392274.
Gardemann, A., Schimkat, D., & Heldt, H. W. (1986). Control of CO2 fixation regulation of stromal fructose-1,6-bisphosphatase in spinach by pH and Mg(2+) concentration. Planta, 168(4), 536-45. https://doi.org/10.1007/BF00392274
Gardemann, A, et al. "Control of CO2 fixation regulation of stromal fructose-1,6-bisphosphatase in spinach by pH and Mg(2+) concentration." Planta vol. 168,4 (1986): 536-45. doi: https://doi.org/10.1007/BF00392274
Gardemann A, Schimkat D, Heldt HW. Control of CO2 fixation regulation of stromal fructose-1,6-bisphosphatase in spinach by pH and Mg(2+) concentration. Planta. 1986 Sep;168(4):536-45. doi: 10.1007/BF00392274. PMID: 24232331.
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Combinatorial Chemistry in the Commercial Jungle.

Angewandte Chemie (International ed. in English)

Rademann J.
PMID: 11458385
Angew Chem Int Ed Engl. 2001 Jul 16;40(14):2721. doi: 10.1002/1521-3773(20010716)40:14<2721::aid-anie2721>3.0.co;2-2.

No abstract available.

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Rademann J. Combinatorial Chemistry in the Commercial Jungle. Angew Chem Int Ed Engl. 2001;40(14):2721doi: 10.1002/1521-3773(20010716)40:14<2721::aid-anie2721>3.0.co;2-2.
Rademann, J. (2001). Combinatorial Chemistry in the Commercial Jungle. Angewandte Chemie (International ed. in English), 40(14), 2721. https://doi.org/10.1002/1521-3773(20010716)40:14<2721::aid-anie2721>3.0.co;2-2
Rademann, Jörg. "Combinatorial Chemistry in the Commercial Jungle." Angewandte Chemie (International ed. in English) vol. 40,14 (2001): 2721. doi: https://doi.org/10.1002/1521-3773(20010716)40:14<2721::aid-anie2721>3.0.co;2-2
Rademann J. Combinatorial Chemistry in the Commercial Jungle. Angew Chem Int Ed Engl. 2001 Jul 16;40(14):2721. doi: 10.1002/1521-3773(20010716)40:14<2721::aid-anie2721>3.0.co;2-2. PMID: 11458385.
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Crystalline structures of Sb4 molecules in antimony thin films.

Angewandte Chemie (International ed. in English)

Bernhardt TM, Stegemann B, Kaiser B, Rademann K.
PMID: 12532349
Angew Chem Int Ed Engl. 2003 Jan 13;42(2):199-202. doi: 10.1002/anie.200390077.

No abstract available.

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Bernhardt TM, Stegemann B, Kaiser B, et al. Crystalline structures of Sb4 molecules in antimony thin films. Angew Chem Int Ed Engl. 2003;42(2):199-202doi: 10.1002/anie.200390077.
Bernhardt, T. M., Stegemann, B., Kaiser, B., & Rademann, K. (2003). Crystalline structures of Sb4 molecules in antimony thin films. Angewandte Chemie (International ed. in English), 42(2), 199-202. https://doi.org/10.1002/anie.200390077
Bernhardt, Thorsten M, et al. "Crystalline structures of Sb4 molecules in antimony thin films." Angewandte Chemie (International ed. in English) vol. 42,2 (2003): 199-202. doi: https://doi.org/10.1002/anie.200390077
Bernhardt TM, Stegemann B, Kaiser B, Rademann K. Crystalline structures of Sb4 molecules in antimony thin films. Angew Chem Int Ed Engl. 2003 Jan 13;42(2):199-202. doi: 10.1002/anie.200390077. PMID: 12532349.
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(68)(28)Ni(40): Magicity versus superfluidity.

Physical review letters

Sorlin O, Leenhardt S, Donzaud C, Duprat J, Azaiez F, Nowacki F, Grawe H, Dombrádi Z, Amorini F, Astier A, Baiborodin D, Belleguic M, Borcea C, Bourgeois C, Cullen DM, Dlouhy Z, Dragulescu E, Górska M, Grévy S, Guillemaud-Mueller D, Hagemann G, Herskind B, Kiener J, Lemmon R, Lewitowicz M, Lukyanov SM, Mayet P, de Oliveira Santos F, Pantalica D, Penionzhkevich YE, Pougheon F, Poves A, Redon N, Saint-Laurent MG, Scarpaci JA, Sletten G, Stanoiu M, Tarasov O, Theisen Ch.
PMID: 11863997
Phys Rev Lett. 2002 Mar 04;88(9):092501. doi: 10.1103/PhysRevLett.88.092501. Epub 2002 Feb 15.

The neutron-rich (66,68)Ni have been produced at GANIL via interactions of a 65.9A MeV 70Zn beam with a 58Ni target. Their reduced transition probability B(E2;0(+)(1)-->2+) has been measured for the first time by Coulomb excitation in a (208)Pb target...

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Sorlin O, Leenhardt S, Donzaud C, et al. (68)(28)Ni(40): Magicity versus superfluidity. Phys Rev Lett. 2002;88(9):092501doi: 10.1103/PhysRevLett.88.092501.
Sorlin, O., Leenhardt, S., Donzaud, C., Duprat, J., Azaiez, F., Nowacki, F., Grawe, H., Dombrádi, Z., Amorini, F., Astier, A., Baiborodin, D., Belleguic, M., Borcea, C., Bourgeois, C., Cullen, D. M., Dlouhy, Z., Dragulescu, E., Górska, M., Grévy, S., Guillemaud-Mueller, D., Hagemann, G., Herskind, B., Kiener, J., Lemmon, R., Lewitowicz, M., Lukyanov, S. M., Mayet, P., de Oliveira Santos, F., Pantalica, D., Penionzhkevich, Y. E., Pougheon, F., Poves, A., Redon, N., Saint-Laurent, M. G., Scarpaci, J. A., Sletten, G., Stanoiu, M., Tarasov, O., & Theisen, C. h. (2002). (68)(28)Ni(40): Magicity versus superfluidity. Physical review letters, 88(9), 092501. https://doi.org/10.1103/PhysRevLett.88.092501
Sorlin, O, et al. "(68)(28)Ni(40): Magicity versus superfluidity." Physical review letters vol. 88,9 (2002): 092501. doi: https://doi.org/10.1103/PhysRevLett.88.092501
Sorlin O, Leenhardt S, Donzaud C, Duprat J, Azaiez F, Nowacki F, Grawe H, Dombrádi Z, Amorini F, Astier A, Baiborodin D, Belleguic M, Borcea C, Bourgeois C, Cullen DM, Dlouhy Z, Dragulescu E, Górska M, Grévy S, Guillemaud-Mueller D, Hagemann G, Herskind B, Kiener J, Lemmon R, Lewitowicz M, Lukyanov SM, Mayet P, de Oliveira Santos F, Pantalica D, Penionzhkevich YE, Pougheon F, Poves A, Redon N, Saint-Laurent MG, Scarpaci JA, Sletten G, Stanoiu M, Tarasov O, Theisen Ch. (68)(28)Ni(40): Magicity versus superfluidity. Phys Rev Lett. 2002 Mar 04;88(9):092501. doi: 10.1103/PhysRevLett.88.092501. Epub 2002 Feb 15. PMID: 11863997.
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