Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 146 entries
Sorted by: Best Match Show Resources per page
Generation of Dicoordinate Boron(I) Units by Fragmentation of a Tetra-Boron(I) Molecular Square.

Angewandte Chemie (International ed. in English)

Arrowsmith M, Auerhammer D, Bertermann R, Braunschweig H, Bringmann G, Celik MA, Dewhurst RD, Finze M, Grüne M, Hailmann M, Hertle T, Krummenacher I.
PMID: 27730749
Angew Chem Int Ed Engl. 2016 Nov 07;55(46):14464-14468. doi: 10.1002/anie.201608429. Epub 2016 Oct 12.

Reduction of carbene-borane adduct [(cAAC)BBr

Cite
Arrowsmith M, Auerhammer D, Bertermann R, et al. Generation of Dicoordinate Boron(I) Units by Fragmentation of a Tetra-Boron(I) Molecular Square. Angew Chem Int Ed Engl. 2016;55(46):14464-14468doi: 10.1002/anie.201608429.
Arrowsmith, M., Auerhammer, D., Bertermann, R., Braunschweig, H., Bringmann, G., Celik, M. A., Dewhurst, R. D., Finze, M., Grüne, M., Hailmann, M., Hertle, T., & Krummenacher, I. (2016). Generation of Dicoordinate Boron(I) Units by Fragmentation of a Tetra-Boron(I) Molecular Square. Angewandte Chemie (International ed. in English), 55(46), 14464-14468. https://doi.org/10.1002/anie.201608429
Arrowsmith, Merle, et al. "Generation of Dicoordinate Boron(I) Units by Fragmentation of a Tetra-Boron(I) Molecular Square." Angewandte Chemie (International ed. in English) vol. 55,46 (2016): 14464-14468. doi: https://doi.org/10.1002/anie.201608429
Arrowsmith M, Auerhammer D, Bertermann R, Braunschweig H, Bringmann G, Celik MA, Dewhurst RD, Finze M, Grüne M, Hailmann M, Hertle T, Krummenacher I. Generation of Dicoordinate Boron(I) Units by Fragmentation of a Tetra-Boron(I) Molecular Square. Angew Chem Int Ed Engl. 2016 Nov 07;55(46):14464-14468. doi: 10.1002/anie.201608429. Epub 2016 Oct 12. PMID: 27730749.
Copy Download .nbib Format: NLM
Nitrogen fixation and reduction at boron.

Science (New York, N.Y.)

Légaré MA, Bélanger-Chabot G, Dewhurst RD, Welz E, Krummenacher I, Engels B, Braunschweig H.
PMID: 29472479
Science. 2018 Feb 23;359(6378):896-900. doi: 10.1126/science.aaq1684.

Currently, the only compounds known to support fixation and functionalization of dinitrogen (N

Cite
Légaré MA, Bélanger-Chabot G, Dewhurst RD, et al. Nitrogen fixation and reduction at boron. Science. 2018;359(6378):896-900doi: 10.1126/science.aaq1684.
Légaré, M. A., Bélanger-Chabot, G., Dewhurst, R. D., Welz, E., Krummenacher, I., Engels, B., & Braunschweig, H. (2018). Nitrogen fixation and reduction at boron. Science (New York, N.Y.), 359(6378), 896-900. https://doi.org/10.1126/science.aaq1684
Légaré, Marc-André, et al. "Nitrogen fixation and reduction at boron." Science (New York, N.Y.) vol. 359,6378 (2018): 896-900. doi: https://doi.org/10.1126/science.aaq1684
Légaré MA, Bélanger-Chabot G, Dewhurst RD, Welz E, Krummenacher I, Engels B, Braunschweig H. Nitrogen fixation and reduction at boron. Science. 2018 Feb 23;359(6378):896-900. doi: 10.1126/science.aaq1684. PMID: 29472479.
Copy Download .nbib Format: NLM
Computational Metabolomics Operations at BioCyc.org.

Metabolites

Karp PD, Billington R, Holland TA, Kothari A, Krummenacker M, Weaver D, Latendresse M, Paley S.
PMID: 26011592
Metabolites. 2015 May 22;5(2):291-310. doi: 10.3390/metabo5020291.

BioCyc.org is a genome and metabolic pathway web portal covering 5500 organisms, including Homo sapiens, Arabidopsis thaliana, Saccharomyces cerevisiae and Escherichia coli. These organism-specific databases have undergone variable degrees of curation. The EcoCyc (Escherichia coli Encyclopedia) database is the...

Cite
Karp PD, Billington R, Holland TA, et al. Computational Metabolomics Operations at BioCyc.org. Metabolites. 2015;5(2):291-310doi: 10.3390/metabo5020291.
Karp, P. D., Billington, R., Holland, T. A., Kothari, A., Krummenacker, M., Weaver, D., Latendresse, M., & Paley, S. (2015). Computational Metabolomics Operations at BioCyc.org. Metabolites, 5(2), 291-310. https://doi.org/10.3390/metabo5020291
Karp, Peter D, et al. "Computational Metabolomics Operations at BioCyc.org." Metabolites vol. 5,2 (2015): 291-310. doi: https://doi.org/10.3390/metabo5020291
Karp PD, Billington R, Holland TA, Kothari A, Krummenacker M, Weaver D, Latendresse M, Paley S. Computational Metabolomics Operations at BioCyc.org. Metabolites. 2015 May 22;5(2):291-310. doi: 10.3390/metabo5020291. PMID: 26011592; PMCID: PMC4495374.
Copy Download .nbib Format: NLM
Isolation of a neutral boron-containing radical stabilized by a cyclic (alkyl)(amino)carbene.

Angewandte Chemie (International ed. in English)

Bissinger P, Braunschweig H, Damme A, Krummenacher I, Phukan AK, Radacki K, Sugawara S.
PMID: 24917474
Angew Chem Int Ed Engl. 2014 Jul 07;53(28):7360-3. doi: 10.1002/anie.201403514. Epub 2014 Jun 10.

Utilizing a cyclic (alkyl)(amino)carbene (CAAC) as a ligand, neutral CAAC-stabilized radicals containing a boryl functionality could be prepared by reduction of the corresponding haloborane adducts. The radical species with a duryl substituent was fully characterized by single-crystal X-ray structural...

Cite
Bissinger P, Braunschweig H, Damme A, et al. Isolation of a neutral boron-containing radical stabilized by a cyclic (alkyl)(amino)carbene. Angew Chem Int Ed Engl. 2014;53(28):7360-3doi: 10.1002/anie.201403514.
Bissinger, P., Braunschweig, H., Damme, A., Krummenacher, I., Phukan, A. K., Radacki, K., & Sugawara, S. (2014). Isolation of a neutral boron-containing radical stabilized by a cyclic (alkyl)(amino)carbene. Angewandte Chemie (International ed. in English), 53(28), 7360-3. https://doi.org/10.1002/anie.201403514
Bissinger, Philipp, et al. "Isolation of a neutral boron-containing radical stabilized by a cyclic (alkyl)(amino)carbene." Angewandte Chemie (International ed. in English) vol. 53,28 (2014): 7360-3. doi: https://doi.org/10.1002/anie.201403514
Bissinger P, Braunschweig H, Damme A, Krummenacher I, Phukan AK, Radacki K, Sugawara S. Isolation of a neutral boron-containing radical stabilized by a cyclic (alkyl)(amino)carbene. Angew Chem Int Ed Engl. 2014 Jul 07;53(28):7360-3. doi: 10.1002/anie.201403514. Epub 2014 Jun 10. PMID: 24917474.
Copy Download .nbib Format: NLM
A theoretical study of the aromaticity in neutral and anionic borole compounds.

Dalton transactions (Cambridge, England : 2003)

Jimenez-Halla JO, Matito E, Solà M, Braunschweig H, Hörl C, Krummenacher I, Wahler J.
PMID: 25494445
Dalton Trans. 2015 Apr 21;44(15):6740-7. doi: 10.1039/c4dt03445g.

In this contribution, we have evaluated the (anti)aromatic character of thirty-four different borole compounds in their neutral and reduced states based on two aromaticity indices, namely nucleus-independent chemical shift (NICS) and multicenter indices (MCI), calculated at the PBE0/6-31+G(d,p) level...

Cite
Jimenez-Halla JO, Matito E, Solà M, et al. A theoretical study of the aromaticity in neutral and anionic borole compounds. Dalton Trans. 2015;44(15):6740-7doi: 10.1039/c4dt03445g.
Jimenez-Halla, J. O., Matito, E., Solà, M., Braunschweig, H., Hörl, C., Krummenacher, I., & Wahler, J. (2015). A theoretical study of the aromaticity in neutral and anionic borole compounds. Dalton transactions (Cambridge, England : 2003), 44(15), 6740-7. https://doi.org/10.1039/c4dt03445g
Jimenez-Halla, J Oscar C, et al. "A theoretical study of the aromaticity in neutral and anionic borole compounds." Dalton transactions (Cambridge, England : 2003) vol. 44,15 (2015): 6740-7. doi: https://doi.org/10.1039/c4dt03445g
Jimenez-Halla JO, Matito E, Solà M, Braunschweig H, Hörl C, Krummenacher I, Wahler J. A theoretical study of the aromaticity in neutral and anionic borole compounds. Dalton Trans. 2015 Apr 21;44(15):6740-7. doi: 10.1039/c4dt03445g. PMID: 25494445.
Copy Download .nbib Format: NLM
Isomerization polymerization of the phosphaalkene MesP=CPh2: an alternative microstructure for poly(methylenephosphine)s.

Angewandte Chemie (International ed. in English)

Siu PW, Serin SC, Krummenacher I, Hey TW, Gates DP.
PMID: 23740733
Angew Chem Int Ed Engl. 2013 Jul 01;52(27):6967-70. doi: 10.1002/anie.201301881. Epub 2013 Jun 05.

No abstract available.

Cite
Siu PW, Serin SC, Krummenacher I, et al. Isomerization polymerization of the phosphaalkene MesP=CPh2: an alternative microstructure for poly(methylenephosphine)s. Angew Chem Int Ed Engl. 2013;52(27):6967-70doi: 10.1002/anie.201301881.
Siu, P. W., Serin, S. C., Krummenacher, I., Hey, T. W., & Gates, D. P. (2013). Isomerization polymerization of the phosphaalkene MesP=CPh2: an alternative microstructure for poly(methylenephosphine)s. Angewandte Chemie (International ed. in English), 52(27), 6967-70. https://doi.org/10.1002/anie.201301881
Siu, Paul W, et al. "Isomerization polymerization of the phosphaalkene MesP=CPh2: an alternative microstructure for poly(methylenephosphine)s." Angewandte Chemie (International ed. in English) vol. 52,27 (2013): 6967-70. doi: https://doi.org/10.1002/anie.201301881
Siu PW, Serin SC, Krummenacher I, Hey TW, Gates DP. Isomerization polymerization of the phosphaalkene MesP=CPh2: an alternative microstructure for poly(methylenephosphine)s. Angew Chem Int Ed Engl. 2013 Jul 01;52(27):6967-70. doi: 10.1002/anie.201301881. Epub 2013 Jun 05. PMID: 23740733.
Copy Download .nbib Format: NLM
Ansa-Complexes of [Mn(η(5) -C5 H5 )(η(6) -C6 H6 )]: Preparation, Characterization, and Reactivity of [n]Manganoarenophanes (n=1, 2, 3).

Chemistry (Weinheim an der Bergstrasse, Germany)

Braunschweig H, Damme A, Dück K, Fuß M, Hörl C, Kramer T, Krummenacher I, Kupfer T, Paprocki V, Schneider C.
PMID: 26387512
Chemistry. 2015 Oct 12;21(42):14797-803. doi: 10.1002/chem.201502161. Epub 2015 Aug 31.

We report the synthesis of [n]manganoarenophanes (n=1, 2) featuring boron, silicon, germanium, and tin as ansa-bridging elements. Their preparation was achieved by salt-elimination reactions of the dilithiated precursor [Mn(η(5) -C5 H4 Li)(η(6) -C6 H5 Li)]⋅pmdta (pmdta=N,N,N',N',N''-pentamethyldiethylenetriamine) with corresponding element...

Cite
Braunschweig H, Damme A, Dück K, et al. Ansa-Complexes of [Mn(η(5) -C5 H5 )(η(6) -C6 H6 )]: Preparation, Characterization, and Reactivity of [n]Manganoarenophanes (n=1, 2, 3). Chemistry. 2015;21(42):14797-803doi: 10.1002/chem.201502161.
Braunschweig, H., Damme, A., Dück, K., Fuß, M., Hörl, C., Kramer, T., Krummenacher, I., Kupfer, T., Paprocki, V., & Schneider, C. (2015). Ansa-Complexes of [Mn(η(5) -C5 H5 )(η(6) -C6 H6 )]: Preparation, Characterization, and Reactivity of [n]Manganoarenophanes (n=1, 2, 3). Chemistry (Weinheim an der Bergstrasse, Germany), 21(42), 14797-803. https://doi.org/10.1002/chem.201502161
Braunschweig, Holger, et al. "Ansa-Complexes of [Mn(η(5) -C5 H5 )(η(6) -C6 H6 )]: Preparation, Characterization, and Reactivity of [n]Manganoarenophanes (n=1, 2, 3)." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,42 (2015): 14797-803. doi: https://doi.org/10.1002/chem.201502161
Braunschweig H, Damme A, Dück K, Fuß M, Hörl C, Kramer T, Krummenacher I, Kupfer T, Paprocki V, Schneider C. Ansa-Complexes of [Mn(η(5) -C5 H5 )(η(6) -C6 H6 )]: Preparation, Characterization, and Reactivity of [n]Manganoarenophanes (n=1, 2, 3). Chemistry. 2015 Oct 12;21(42):14797-803. doi: 10.1002/chem.201502161. Epub 2015 Aug 31. PMID: 26387512.
Copy Download .nbib Format: NLM
Aminotroponiminates as tunable, redox-active ligands: reversible single electron transfer and reductive dimerisation.

Chemical communications (Cambridge, England)

Lichtenberg C, Krummenacher I.
PMID: 27452905
Chem Commun (Camb). 2016 Aug 21;52(65):10044-7. doi: 10.1039/c6cc05762d. Epub 2016 Jul 25.

Aminotroponiminates (atis) are shown to be redox-active ligands. Under strongly reducing conditions, the result of electron transfer can be controlled by the choice of the metal bound to the ati ligand. Either reversible electron transfer or a reductively induced...

Cite
Lichtenberg C, Krummenacher I. Aminotroponiminates as tunable, redox-active ligands: reversible single electron transfer and reductive dimerisation. Chem Commun (Camb). 2016;52(65):10044-7doi: 10.1039/c6cc05762d.
Lichtenberg, C., & Krummenacher, I. (2016). Aminotroponiminates as tunable, redox-active ligands: reversible single electron transfer and reductive dimerisation. Chemical communications (Cambridge, England), 52(65), 10044-7. https://doi.org/10.1039/c6cc05762d
Lichtenberg, C, and Krummenacher, I. "Aminotroponiminates as tunable, redox-active ligands: reversible single electron transfer and reductive dimerisation." Chemical communications (Cambridge, England) vol. 52,65 (2016): 10044-7. doi: https://doi.org/10.1039/c6cc05762d
Lichtenberg C, Krummenacher I. Aminotroponiminates as tunable, redox-active ligands: reversible single electron transfer and reductive dimerisation. Chem Commun (Camb). 2016 Aug 21;52(65):10044-7. doi: 10.1039/c6cc05762d. Epub 2016 Jul 25. PMID: 27452905.
Copy Download .nbib Format: NLM
Multidentate ligand systems featuring dual functionality.

Dalton transactions (Cambridge, England : 2003)

Kuzu I, Krummenacher I, Meyer J, Armbruster F, Breher F.
PMID: 19082036
Dalton Trans. 2008 Nov 21;(43):5836-65. doi: 10.1039/b808347a. Epub 2008 Oct 01.

Multifunctional ligands with podand topology provide intrinsically well-defined coordination geometries. Several subgroups of multidentate ligand systems comprising dual functionality have been developed so far. Recent advances made in this research area reflect its topicality. Work on metal complexes of...

Cite
Kuzu I, Krummenacher I, Meyer J, et al. Multidentate ligand systems featuring dual functionality. Dalton Trans. 2008;(43):5836-65doi: 10.1039/b808347a.
Kuzu, I., Krummenacher, I., Meyer, J., Armbruster, F., & Breher, F. (2008). Multidentate ligand systems featuring dual functionality. Dalton transactions (Cambridge, England : 2003), (43), 5836-65. https://doi.org/10.1039/b808347a
Kuzu, Istemi, et al. "Multidentate ligand systems featuring dual functionality." Dalton transactions (Cambridge, England : 2003) vol. ,43 (2008): 5836-65. doi: https://doi.org/10.1039/b808347a
Kuzu I, Krummenacher I, Meyer J, Armbruster F, Breher F. Multidentate ligand systems featuring dual functionality. Dalton Trans. 2008 Nov 21;(43):5836-65. doi: 10.1039/b808347a. Epub 2008 Oct 01. PMID: 19082036.
Copy Download .nbib Format: NLM
Coinage metal complexes of tris(pyrazolyl)methanide [C(3,5-Me2pz)3]-: kappa3-coordination vs. backbone functionalisation.

Dalton transactions (Cambridge, England : 2003)

Krummenacher I, Rüegger H, Breher F.
PMID: 16474893
Dalton Trans. 2006 Feb 28;(8):1073-81. doi: 10.1039/b512309g. Epub 2005 Nov 28.

Tris(pyrazolyl)methanides, [C(3,5-R2pz)3]-, contain an unassociated tetrahedral carbanionic centre in the bridgehead position. In addition to nitrogen donor centres for transition metal coordination, an accessible reactive site for further manipulations is available in the backbone of the ligand. The coordination...

Cite
Krummenacher I, Rüegger H, Breher F. Coinage metal complexes of tris(pyrazolyl)methanide [C(3,5-Me2pz)3]-: kappa3-coordination vs. backbone functionalisation. Dalton Trans. 2005;(8):1073-81doi: 10.1039/b512309g.
Krummenacher, I., Rüegger, H., & Breher, F. (2006). Coinage metal complexes of tris(pyrazolyl)methanide [C(3,5-Me2pz)3]-: kappa3-coordination vs. backbone functionalisation. Dalton transactions (Cambridge, England : 2003), (8), 1073-81. https://doi.org/10.1039/b512309g
Krummenacher, Ivo, et al. "Coinage metal complexes of tris(pyrazolyl)methanide [C(3,5-Me2pz)3]-: kappa3-coordination vs. backbone functionalisation." Dalton transactions (Cambridge, England : 2003) vol. ,8 (2006): 1073-81. doi: https://doi.org/10.1039/b512309g
Krummenacher I, Rüegger H, Breher F. Coinage metal complexes of tris(pyrazolyl)methanide [C(3,5-Me2pz)3]-: kappa3-coordination vs. backbone functionalisation. Dalton Trans. 2006 Feb 28;(8):1073-81. doi: 10.1039/b512309g. Epub 2005 Nov 28. PMID: 16474893.
Copy Download .nbib Format: NLM
Synthesis, coordination behavior, and reduction chemistry of cymantrenyl-1,3-bis(2,3,4,5-tetraphenyl)borole.

Chemistry (Weinheim an der Bergstrasse, Germany)

Braunschweig H, Damme A, Gamon D, Kelch H, Krummenacher I, Kupfer T, Radacki K.
PMID: 22639411
Chemistry. 2012 Jul 02;18(27):8430-6. doi: 10.1002/chem.201200284. Epub 2012 May 25.

We describe the synthesis of base-free bisborole [Cym(†)(BC(4)Ph(4))(2)]-Cym(†)=(OC)(3)Mn(η(5)-C(5)H(3))-and its transformation into two fully characterized Lewis acid-base adducts with pyridine bases of the type 4-R-NC(5)H(4) (R=tBu, NMe(2)). The results of electrochemical, as well as NMR and UV/Vis spectroscopic studies on...

Cite
Braunschweig H, Damme A, Gamon D, et al. Synthesis, coordination behavior, and reduction chemistry of cymantrenyl-1,3-bis(2,3,4,5-tetraphenyl)borole. Chemistry. 2012;18(27):8430-6doi: 10.1002/chem.201200284.
Braunschweig, H., Damme, A., Gamon, D., Kelch, H., Krummenacher, I., Kupfer, T., & Radacki, K. (2012). Synthesis, coordination behavior, and reduction chemistry of cymantrenyl-1,3-bis(2,3,4,5-tetraphenyl)borole. Chemistry (Weinheim an der Bergstrasse, Germany), 18(27), 8430-6. https://doi.org/10.1002/chem.201200284
Braunschweig, Holger, et al. "Synthesis, coordination behavior, and reduction chemistry of cymantrenyl-1,3-bis(2,3,4,5-tetraphenyl)borole." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 18,27 (2012): 8430-6. doi: https://doi.org/10.1002/chem.201200284
Braunschweig H, Damme A, Gamon D, Kelch H, Krummenacher I, Kupfer T, Radacki K. Synthesis, coordination behavior, and reduction chemistry of cymantrenyl-1,3-bis(2,3,4,5-tetraphenyl)borole. Chemistry. 2012 Jul 02;18(27):8430-6. doi: 10.1002/chem.201200284. Epub 2012 May 25. PMID: 22639411.
Copy Download .nbib Format: NLM
Construction and completion of flux balance models from pathway databases.

Bioinformatics (Oxford, England)

Latendresse M, Krummenacker M, Trupp M, Karp PD.
PMID: 22262672
Bioinformatics. 2012 Feb 01;28(3):388-96. doi: 10.1093/bioinformatics/btr681. Epub 2012 Jan 18.

MOTIVATION: Flux balance analysis (FBA) is a well-known technique for genome-scale modeling of metabolic flux. Typically, an FBA formulation requires the accurate specification of four sets: biochemical reactions, biomass metabolites, nutrients and secreted metabolites. The development of FBA models...

Cite
Latendresse M, Krummenacker M, Trupp M, et al. Construction and completion of flux balance models from pathway databases. Bioinformatics. 2012;28(3):388-96doi: 10.1093/bioinformatics/btr681.
Latendresse, M., Krummenacker, M., Trupp, M., & Karp, P. D. (2012). Construction and completion of flux balance models from pathway databases. Bioinformatics (Oxford, England), 28(3), 388-96. https://doi.org/10.1093/bioinformatics/btr681
Latendresse, Mario, et al. "Construction and completion of flux balance models from pathway databases." Bioinformatics (Oxford, England) vol. 28,3 (2012): 388-96. doi: https://doi.org/10.1093/bioinformatics/btr681
Latendresse M, Krummenacker M, Trupp M, Karp PD. Construction and completion of flux balance models from pathway databases. Bioinformatics. 2012 Feb 01;28(3):388-96. doi: 10.1093/bioinformatics/btr681. Epub 2012 Jan 18. PMID: 22262672; PMCID: PMC3268246.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 146 entries