Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 197 entries
Sorted by: Best Match Show Resources per page
Mechanistic Aspects of Redox-Induced Assembly and Disassembly of S-Bridged [2M-2S] Structures.

Chemistry (Weinheim an der Bergstrasse, Germany)

Koch F, Berkefeld A, Speiser B, Schubert H.
PMID: 28976037
Chemistry. 2017 Nov 21;23(65):16681-16690. doi: 10.1002/chem.201704599. Epub 2017 Nov 09.

Sulfur-bridged binuclear structures [2M-2S] play a pivotal role in a variety of chemical processes such as bond breaking and formation and electron transfer. In general, structural persistence is deemed essential to the respective function but owing to the lack...

Cite
Koch F, Berkefeld A, Speiser B, et al. Mechanistic Aspects of Redox-Induced Assembly and Disassembly of S-Bridged [2M-2S] Structures. Chemistry. 2017;23(65):16681-16690doi: 10.1002/chem.201704599.
Koch, F., Berkefeld, A., Speiser, B., & Schubert, H. (2017). Mechanistic Aspects of Redox-Induced Assembly and Disassembly of S-Bridged [2M-2S] Structures. Chemistry (Weinheim an der Bergstrasse, Germany), 23(65), 16681-16690. https://doi.org/10.1002/chem.201704599
Koch, Felix, et al. "Mechanistic Aspects of Redox-Induced Assembly and Disassembly of S-Bridged [2M-2S] Structures." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 23,65 (2017): 16681-16690. doi: https://doi.org/10.1002/chem.201704599
Koch F, Berkefeld A, Speiser B, Schubert H. Mechanistic Aspects of Redox-Induced Assembly and Disassembly of S-Bridged [2M-2S] Structures. Chemistry. 2017 Nov 21;23(65):16681-16690. doi: 10.1002/chem.201704599. Epub 2017 Nov 09. PMID: 28976037.
Copy Download .nbib Format: NLM
Direct measurement of individual phonon lifetimes in the clathrate compound Ba.

Nature communications

Lory PF, Pailhès S, Giordano VM, Euchner H, Nguyen HD, Ramlau R, Borrmann H, Schmidt M, Baitinger M, Ikeda M, Tomeš P, Mihalkovič M, Allio C, Johnson MR, Schober H, Sidis Y, Bourdarot F, Regnault LP, Ollivier J, Paschen S, Grin Y, de Boissieu M.
PMID: 28887470
Nat Commun. 2017 Sep 08;8(1):491. doi: 10.1038/s41467-017-00584-7.

Engineering lattice thermal conductivity requires to control the heat carried by atomic vibration waves, the phonons. The key parameter for quantifying it is the phonon lifetime, limiting the travelling distance, whose determination is however at the limits of instrumental...

Cite
Lory PF, Pailhès S, Giordano VM, et al. Direct measurement of individual phonon lifetimes in the clathrate compound Ba. Nat Commun. 2017;8(1):491doi: 10.1038/s41467-017-00584-7.
Lory, P. F., Pailhès, S., Giordano, V. M., Euchner, H., Nguyen, H. D., Ramlau, R., Borrmann, H., Schmidt, M., Baitinger, M., Ikeda, M., Tomeš, P., Mihalkovič, M., Allio, C., Johnson, M. R., Schober, H., Sidis, Y., Bourdarot, F., Regnault, L. P., Ollivier, J., Paschen, S., Grin, Y., & de Boissieu, M. (2017). Direct measurement of individual phonon lifetimes in the clathrate compound Ba. Nature communications, 8(1), 491. https://doi.org/10.1038/s41467-017-00584-7
Lory, Pierre-François, et al. "Direct measurement of individual phonon lifetimes in the clathrate compound Ba." Nature communications vol. 8,1 (2017): 491. doi: https://doi.org/10.1038/s41467-017-00584-7
Lory PF, Pailhès S, Giordano VM, Euchner H, Nguyen HD, Ramlau R, Borrmann H, Schmidt M, Baitinger M, Ikeda M, Tomeš P, Mihalkovič M, Allio C, Johnson MR, Schober H, Sidis Y, Bourdarot F, Regnault LP, Ollivier J, Paschen S, Grin Y, de Boissieu M. Direct measurement of individual phonon lifetimes in the clathrate compound Ba. Nat Commun. 2017 Sep 08;8(1):491. doi: 10.1038/s41467-017-00584-7. PMID: 28887470; PMCID: PMC5591192.
Copy Download .nbib Format: NLM
η(3) -Allyl coordination at tin(II)-reactivity towards alkynes and benzonitrile.

Angewandte Chemie (International ed. in English)

Krebs KM, Wiederkehr J, Schneider J, Schubert H, Eichele K, Wesemann L.
PMID: 25766048
Angew Chem Int Ed Engl. 2015 Apr 27;54(18):5502-6. doi: 10.1002/anie.201500386. Epub 2015 Mar 12.

We herein report the synthesis and characterization of a terphenyl-substituted Sn(II) allyl compound featuring an η(3)  coordination mode in solution and in the solid state. Two examples for the interesting reactivity of the allyl Sn(II) molecule are presented: Reactions...

Cite
Krebs KM, Wiederkehr J, Schneider J, et al. η(3) -Allyl coordination at tin(II)-reactivity towards alkynes and benzonitrile. Angew Chem Int Ed Engl. 2015;54(18):5502-6doi: 10.1002/anie.201500386.
Krebs, K. M., Wiederkehr, J., Schneider, J., Schubert, H., Eichele, K., & Wesemann, L. (2015). η(3) -Allyl coordination at tin(II)-reactivity towards alkynes and benzonitrile. Angewandte Chemie (International ed. in English), 54(18), 5502-6. https://doi.org/10.1002/anie.201500386
Krebs, Kilian M, et al. "η(3) -Allyl coordination at tin(II)-reactivity towards alkynes and benzonitrile." Angewandte Chemie (International ed. in English) vol. 54,18 (2015): 5502-6. doi: https://doi.org/10.1002/anie.201500386
Krebs KM, Wiederkehr J, Schneider J, Schubert H, Eichele K, Wesemann L. η(3) -Allyl coordination at tin(II)-reactivity towards alkynes and benzonitrile. Angew Chem Int Ed Engl. 2015 Apr 27;54(18):5502-6. doi: 10.1002/anie.201500386. Epub 2015 Mar 12. PMID: 25766048.
Copy Download .nbib Format: NLM
Chemistry of stannylene-based Lewis pairs: dynamic tin coordination switching between donor and acceptor character.

Chemistry (Weinheim an der Bergstrasse, Germany)

Krebs KM, Freitag S, Schubert H, Gerke B, Pöttgen R, Wesemann L.
PMID: 25677701
Chemistry. 2015 Mar 16;21(12):4628-38. doi: 10.1002/chem.201406486. Epub 2015 Feb 11.

The coordination chemistry of cyclic stannylene-based intramolecular Lewis pairs is presented. The P→Sn adducts were treated with [Ni(COD)2] and [Pd(PCy3)2] (COD = 1,5-cyclooctadiene, PCy3 = tricyclohexylphosphine). In the isolated coordination compounds the stannylene moiety acts either as an acceptor...

Cite
Krebs KM, Freitag S, Schubert H, et al. Chemistry of stannylene-based Lewis pairs: dynamic tin coordination switching between donor and acceptor character. Chemistry. 2015;21(12):4628-38doi: 10.1002/chem.201406486.
Krebs, K. M., Freitag, S., Schubert, H., Gerke, B., Pöttgen, R., & Wesemann, L. (2015). Chemistry of stannylene-based Lewis pairs: dynamic tin coordination switching between donor and acceptor character. Chemistry (Weinheim an der Bergstrasse, Germany), 21(12), 4628-38. https://doi.org/10.1002/chem.201406486
Krebs, Kilian M, et al. "Chemistry of stannylene-based Lewis pairs: dynamic tin coordination switching between donor and acceptor character." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,12 (2015): 4628-38. doi: https://doi.org/10.1002/chem.201406486
Krebs KM, Freitag S, Schubert H, Gerke B, Pöttgen R, Wesemann L. Chemistry of stannylene-based Lewis pairs: dynamic tin coordination switching between donor and acceptor character. Chemistry. 2015 Mar 16;21(12):4628-38. doi: 10.1002/chem.201406486. Epub 2015 Feb 11. PMID: 25677701.
Copy Download .nbib Format: NLM
Hydrodabcyl: A Superior Hydrophilic Alternative to the Dark Fluorescence Quencher Dabcyl.

Analytical chemistry

Kempf O, Kempf K, Schobert R, Bombarda E.
PMID: 29069895
Anal Chem. 2017 Nov 21;89(22):11893-11897. doi: 10.1021/acs.analchem.7b03488. Epub 2017 Nov 07.

Dark fluorescence quenchers are nonfluorescent dyes that can modulate the fluorescence signal of an appropriate fluorophore donor in a distance-dependent manner. Dark quenchers are extensively used in many biomolecular analytical applications, such as studies with fluorogenic protease substrates or...

Cite
Kempf O, Kempf K, Schobert R, et al. Hydrodabcyl: A Superior Hydrophilic Alternative to the Dark Fluorescence Quencher Dabcyl. Anal Chem. 2017;89(22):11893-11897doi: 10.1021/acs.analchem.7b03488.
Kempf, O., Kempf, K., Schobert, R., & Bombarda, E. (2017). Hydrodabcyl: A Superior Hydrophilic Alternative to the Dark Fluorescence Quencher Dabcyl. Analytical chemistry, 89(22), 11893-11897. https://doi.org/10.1021/acs.analchem.7b03488
Kempf, Oxana, et al. "Hydrodabcyl: A Superior Hydrophilic Alternative to the Dark Fluorescence Quencher Dabcyl." Analytical chemistry vol. 89,22 (2017): 11893-11897. doi: https://doi.org/10.1021/acs.analchem.7b03488
Kempf O, Kempf K, Schobert R, Bombarda E. Hydrodabcyl: A Superior Hydrophilic Alternative to the Dark Fluorescence Quencher Dabcyl. Anal Chem. 2017 Nov 21;89(22):11893-11897. doi: 10.1021/acs.analchem.7b03488. Epub 2017 Nov 07. PMID: 29069895.
Copy Download .nbib Format: NLM
Superionic conduction in β-eucryptite: inelastic neutron scattering and computational studies.

Physical chemistry chemical physics : PCCP

Singh B, Gupta MK, Mittal R, Zbiri M, Rols S, Patwe SJ, Achary SN, Schober H, Tyagi AK, Chaplot SL.
PMID: 28581550
Phys Chem Chem Phys. 2017 Jun 14;19(23):15512-15520. doi: 10.1039/c7cp01490b.

β-Eucryptite (LiAlSiO

Cite
Singh B, Gupta MK, Mittal R, et al. Superionic conduction in β-eucryptite: inelastic neutron scattering and computational studies. Phys Chem Chem Phys. 2017;19(23):15512-15520doi: 10.1039/c7cp01490b.
Singh, B., Gupta, M. K., Mittal, R., Zbiri, M., Rols, S., Patwe, S. J., Achary, S. N., Schober, H., Tyagi, A. K., & Chaplot, S. L. (2017). Superionic conduction in β-eucryptite: inelastic neutron scattering and computational studies. Physical chemistry chemical physics : PCCP, 19(23), 15512-15520. https://doi.org/10.1039/c7cp01490b
Singh, Baltej, et al. "Superionic conduction in β-eucryptite: inelastic neutron scattering and computational studies." Physical chemistry chemical physics : PCCP vol. 19,23 (2017): 15512-15520. doi: https://doi.org/10.1039/c7cp01490b
Singh B, Gupta MK, Mittal R, Zbiri M, Rols S, Patwe SJ, Achary SN, Schober H, Tyagi AK, Chaplot SL. Superionic conduction in β-eucryptite: inelastic neutron scattering and computational studies. Phys Chem Chem Phys. 2017 Jun 14;19(23):15512-15520. doi: 10.1039/c7cp01490b. PMID: 28581550.
Copy Download .nbib Format: NLM
Reversibility in Reactions of Linker-Bridged Distannenes with Terminal Alkynes at Ambient Temperature.

Inorganic chemistry

Schneider J, Henning J, Edrich J, Schubert H, Wesemann L.
PMID: 26030466
Inorg Chem. 2015 Jun 15;54(12):6020-7. doi: 10.1021/acs.inorgchem.5b00896. Epub 2015 Jun 01.

The linker-bridged distannene [(2,6-Mes2)C6H3Sn]2C12H8 (1) featuring an acenaphthene linker and the sterically demanding terphenyl substituent Ar(Me) (= C6H3-2,6-Mes2; Mes = C6H2-2,4,6-Me3) was prepared and characterized by single-crystal analysis, NMR spectroscopy, as well as elemental analysis. Furthermore, the reactivity of...

Cite
Schneider J, Henning J, Edrich J, et al. Reversibility in Reactions of Linker-Bridged Distannenes with Terminal Alkynes at Ambient Temperature. Inorg Chem. 2015;54(12):6020-7doi: 10.1021/acs.inorgchem.5b00896.
Schneider, J., Henning, J., Edrich, J., Schubert, H., & Wesemann, L. (2015). Reversibility in Reactions of Linker-Bridged Distannenes with Terminal Alkynes at Ambient Temperature. Inorganic chemistry, 54(12), 6020-7. https://doi.org/10.1021/acs.inorgchem.5b00896
Schneider, Julia, et al. "Reversibility in Reactions of Linker-Bridged Distannenes with Terminal Alkynes at Ambient Temperature." Inorganic chemistry vol. 54,12 (2015): 6020-7. doi: https://doi.org/10.1021/acs.inorgchem.5b00896
Schneider J, Henning J, Edrich J, Schubert H, Wesemann L. Reversibility in Reactions of Linker-Bridged Distannenes with Terminal Alkynes at Ambient Temperature. Inorg Chem. 2015 Jun 15;54(12):6020-7. doi: 10.1021/acs.inorgchem.5b00896. Epub 2015 Jun 01. PMID: 26030466.
Copy Download .nbib Format: NLM
Intramolecular Tetrylene Lewis Adducts: Synthesis and Reactivity.

Chemistry (Weinheim an der Bergstrasse, Germany)

Schneider J, Krebs KM, Freitag S, Eichele K, Schubert H, Wesemann L.
PMID: 27273819
Chemistry. 2016 Jul 04;22(28):9812-26. doi: 10.1002/chem.201601224. Epub 2016 Jun 07.

A series of benzyl(diphenylphosphino) and o-phenyl(diphenlyphosphino) substituted germylenes and plumbylenes were synthesized by nucleophilic substitution between the respective lithium reagent and tetrylene halide. The Lewis pairs were characterized by X-ray crystallography and NMR spectroscopy. The reactivity of the tetrylenes...

Cite
Schneider J, Krebs KM, Freitag S, et al. Intramolecular Tetrylene Lewis Adducts: Synthesis and Reactivity. Chemistry. 2016;22(28):9812-26doi: 10.1002/chem.201601224.
Schneider, J., Krebs, K. M., Freitag, S., Eichele, K., Schubert, H., & Wesemann, L. (2016). Intramolecular Tetrylene Lewis Adducts: Synthesis and Reactivity. Chemistry (Weinheim an der Bergstrasse, Germany), 22(28), 9812-26. https://doi.org/10.1002/chem.201601224
Schneider, Julia, et al. "Intramolecular Tetrylene Lewis Adducts: Synthesis and Reactivity." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 22,28 (2016): 9812-26. doi: https://doi.org/10.1002/chem.201601224
Schneider J, Krebs KM, Freitag S, Eichele K, Schubert H, Wesemann L. Intramolecular Tetrylene Lewis Adducts: Synthesis and Reactivity. Chemistry. 2016 Jul 04;22(28):9812-26. doi: 10.1002/chem.201601224. Epub 2016 Jun 07. PMID: 27273819.
Copy Download .nbib Format: NLM
Redox and Acid-Base Properties of Binuclear 4-Terphenyldithiophenolate Complexes of Nickel.

Chemistry (Weinheim an der Bergstrasse, Germany)

Koch F, Berkefeld A, Schubert H, Grauer C.
PMID: 27554625
Chemistry. 2016 Oct 04;22(41):14640-7. doi: 10.1002/chem.201603060. Epub 2016 Aug 24.

This work reports on the redox and acid-base properties of binuclear complexes of nickel from 1,4-terphenyldithiophenol ligands. The results provide insight into the cooperative electronic interaction between a dinickel core and its ligand. Donor/acceptor contributions flexibly adjust to stabilize...

Cite
Koch F, Berkefeld A, Schubert H, et al. Redox and Acid-Base Properties of Binuclear 4-Terphenyldithiophenolate Complexes of Nickel. Chemistry. 2016;22(41):14640-7doi: 10.1002/chem.201603060.
Koch, F., Berkefeld, A., Schubert, H., & Grauer, C. (2016). Redox and Acid-Base Properties of Binuclear 4-Terphenyldithiophenolate Complexes of Nickel. Chemistry (Weinheim an der Bergstrasse, Germany), 22(41), 14640-7. https://doi.org/10.1002/chem.201603060
Koch, Felix, et al. "Redox and Acid-Base Properties of Binuclear 4-Terphenyldithiophenolate Complexes of Nickel." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 22,41 (2016): 14640-7. doi: https://doi.org/10.1002/chem.201603060
Koch F, Berkefeld A, Schubert H, Grauer C. Redox and Acid-Base Properties of Binuclear 4-Terphenyldithiophenolate Complexes of Nickel. Chemistry. 2016 Oct 04;22(41):14640-7. doi: 10.1002/chem.201603060. Epub 2016 Aug 24. PMID: 27554625.
Copy Download .nbib Format: NLM
Déjà vu … All Over Again.

Foot & ankle specialist

Schuberth J.
PMID: 27390288
Foot Ankle Spec. 2016 Aug;9(4):300. doi: 10.1177/1938640016658728. Epub 2016 Jul 07.

No abstract available.

Cite
Schuberth J. Déjà vu … All Over Again. Foot Ankle Spec. 2016;9(4):300doi: 10.1177/1938640016658728.
Schuberth, J. (2016). Déjà vu … All Over Again. Foot & ankle specialist, 9(4), 300. https://doi.org/10.1177/1938640016658728
Schuberth, Jack. "Déjà vu … All Over Again." Foot & ankle specialist vol. 9,4 (2016): 300. doi: https://doi.org/10.1177/1938640016658728
Schuberth J. Déjà vu … All Over Again. Foot Ankle Spec. 2016 Aug;9(4):300. doi: 10.1177/1938640016658728. Epub 2016 Jul 07. PMID: 27390288.
Copy Download .nbib Format: NLM
Krimmel et al. reply:.

Physical review letters

Krimmel A, Loidl A, Klemm M, Horn S, Schober H.
PMID: 11041979
Phys Rev Lett. 2000 Oct 30;85(18):3982. doi: 10.1103/PhysRevLett.85.3982.

No abstract available.

Cite
Krimmel A, Loidl A, Klemm M, et al. Krimmel et al. reply:. Phys Rev Lett. 2000;85(18):3982doi: 10.1103/PhysRevLett.85.3982.
Krimmel, A., Loidl, A., Klemm, M., Horn, S., & Schober, H. (2000). Krimmel et al. reply:. Physical review letters, 85(18), 3982. https://doi.org/10.1103/PhysRevLett.85.3982
Krimmel, et al. "Krimmel et al. reply:." Physical review letters vol. 85,18 (2000): 3982. doi: https://doi.org/10.1103/PhysRevLett.85.3982
Krimmel A, Loidl A, Klemm M, Horn S, Schober H. Krimmel et al. reply:. Phys Rev Lett. 2000 Oct 30;85(18):3982. doi: 10.1103/PhysRevLett.85.3982. PMID: 11041979.
Copy Download .nbib Format: NLM
Germa-closo-dodecaborate: a new ligand in transition-metal chemistry with a strong trans influence.

Chemistry (Weinheim an der Bergstrasse, Germany)

Dimmer JA, Schubert H, Wesemann L.
PMID: 19739218
Chemistry. 2009 Oct 12;15(40):10613-9. doi: 10.1002/chem.200901308.

The strong nucleophilic character of germa-closo-dodecaborate towards late transition metal centres is described. The synthesis and characterisation of the first germa-closo-dodecaborate complexes are presented, and the solid state structures of the germaborate transition metal complexes were determined by X-ray...

Cite
Dimmer JA, Schubert H, Wesemann L. Germa-closo-dodecaborate: a new ligand in transition-metal chemistry with a strong trans influence. Chemistry. 2009;15(40):10613-9doi: 10.1002/chem.200901308.
Dimmer, J. A., Schubert, H., & Wesemann, L. (2009). Germa-closo-dodecaborate: a new ligand in transition-metal chemistry with a strong trans influence. Chemistry (Weinheim an der Bergstrasse, Germany), 15(40), 10613-9. https://doi.org/10.1002/chem.200901308
Dimmer, Jörg-Alexander, et al. "Germa-closo-dodecaborate: a new ligand in transition-metal chemistry with a strong trans influence." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 15,40 (2009): 10613-9. doi: https://doi.org/10.1002/chem.200901308
Dimmer JA, Schubert H, Wesemann L. Germa-closo-dodecaborate: a new ligand in transition-metal chemistry with a strong trans influence. Chemistry. 2009 Oct 12;15(40):10613-9. doi: 10.1002/chem.200901308. PMID: 19739218.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 197 entries