Preise der Chemical Society of Japan 2005 (Deutsch)
In:
Angewandte Chemie
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118
, 17
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2720
;
2006
- Aufsatz (Zeitschrift) / Elektronische Ressource
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Titel:Preise der Chemical Society of Japan 2005
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Erschienen in:Angewandte Chemie ; 118, 17 ; 2720
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Verlag:
- Neue Suche nach: WILEY‐VCH Verlag
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Erscheinungsdatum:21.04.2006
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Format / Umfang:1 pages
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ISSN:
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DOI:
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Medientyp:Aufsatz (Zeitschrift)
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Format:Elektronische Ressource
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Sprache:Deutsch
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Datenquelle:
Inhaltsverzeichnis – Band 118, Ausgabe 17
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Die Inhaltsverzeichnisse werden automatisch erzeugt und basieren auf den im Index des TIB-Portals verfügbaren Einzelnachweisen der enthaltenen Beiträge. Die Anzeige der Inhaltsverzeichnisse kann daher unvollständig oder lückenhaft sein.
- 2705
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Titelbild: Flattened Cone 2,8,14,20‐Tetrakis(L‐valinamido)[4]resorcinarene: An Enantioselective Allosteric Receptor in the Gas Phase (Angew. Chem. 17/2006)Botta, Bruno / Caporuscio, Fabiana / Subissati, Deborah / Tafi, Andrea / Botta, Maurizio / Filippi, Antonello / Speranza, Maurizio et al. | 2006
- 2708
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Graphisches Inhaltsverzeichnis: Angew. Chem. 17/2006| 2006
- 2720
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Preise der Chemical Society of Japan 2005| 2006
- 2721
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The World's Greatest Fix. A History of Nitrogen and Agriculture. Von G. J. Leigh.Fryzuk, Michael D. et al. | 2006
- 2722
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Modern Organonickel Chemistry. Herausgegeben von Yoshinao Tamaru.Masuyama, Yoshiro et al. | 2006
- 2723
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Metapher und Experiment. Von der Virusforschung zum genetischen Code. Von Christina Brandt.Kretzenbacher, Heinz L. et al. | 2006
- 2726
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Dynamische kombinatorische Chemie: die uberraschende Rezeptorwahl durch Gastmolekulede Bruin, B. / Hauwert, P. / Reek, J. N. et al. | 2006
- 2726
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Dynamische kombinatorische Chemie: die überraschende Rezeptorwahl durch Gastmolekülede Bruin, Bas / Hauwert, Peter / Reek, Joost N. H. et al. | 2006
- 2730
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Ringschlussmetathese: ein Schlüssel zur ArensyntheseDonohoe, Timothy J. / Orr, Allan J. / Bingham, Matilda et al. | 2006
- 2730
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Ringschlussmetathese: ein Schlussel zur ArensyntheseDonohoe, T. J. / Orr, A. J. / Bingham, M. et al. | 2006
- 2738
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Vielsegmentige Nanostabe: Templatsynthese und EigenschaftenHurst, S. J. / Payne, E. K. / Qin, L. / Mirkin, C. A. et al. | 2006
- 2738
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Vielsegmentige Nanostäbe: Templatsynthese und EigenschaftenHurst, Sarah J. / Payne, Emma Kathryn / Qin, Lidong / Mirkin, Chad A. et al. | 2006
- 2760
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A Bis(pyridyl)allenylidene Complex of Ruthenium: A "Molecular Clip" That Displays Intense Near-Infrared Absorption upon Coordination to a Ruthenium(II) Center. This work was supported by the Research Grants Council of the Hong Kong SAR, China (HKU 7077-01P) and the University of Hong Kong.Wong, Chun-Yuen et al. | 2006
- 2760
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A Bis(pyridyl)allenylidene Complex of Ruthenium: A “Molecular Clip” That Displays Intense Near‐Infrared Absorption upon Coordination to a Ruthenium(II) CenterWong, Chun‐Yuen / Tong, Glenna So Ming / Che, Chi‐Ming / Zhu, Nianyong et al. | 2006
- 2765
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Control of Amyloid b-Peptide Protofibril Formation by a Designed Template Assembly. We thank Dr. Serge Perez for access to an electron microscope and Isabelle Paintrand for performing the study. This work was supported by grants from AFM-INSERM GIS "maladies rares amyloses héréditaires" (no. AE02013 KSA), IUF, and ACI.Dolphin, Gunnar T. et al. | 2006
- 2765
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Control of Amyloid β‐Peptide Protofibril Formation by a Designed Template AssemblyDolphin, Gunnar T. / Dumy, Pascal / Garcia, Julian et al. | 2006
- 2765
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Control of Amyloid b-Peptide Protofibril Formation by a Designed Template AssemblyDolphin, G. T. / Dumy, P. / Garcia, J. et al. | 2006
- 2769
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DNA Recognition with Large Calixarene Dimers. We are indebted to the Carell group (Munich) for a sample of fluorescein-labeled triadenosine, as well as to the Marahiel group (Marburg) for 45-bp DNA samples. Valuable advice came from Dr. Mohamad Mofid. We also thank the Pingoud group (Giessen) for the measurements of CD spectra. Funding by the Deutsche Forschungsgemeinschaft is gratefully acknowledged.Zadmard, Reza et al. | 2006
- 2769
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DNA Recognition with Large Calixarene DimersZadmard, Reza / Schrader, Thomas et al. | 2006
- 2773
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A Fluorescent Indicator To Visualize Activities of the Androgen Receptor Ligands in Single Living CellsAwais, Muhammad / Sato, Moritoshi / Lee, Xianfen / Umezawa, Yoshio et al. | 2006
- 2773
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A Fluorescent Indicator To Visualize Activities of the Androgen Receptor Ligands in Single Living Cells. This work was supported by grants from the Japan Science and Technology Agency (JST) and the Japan Society for the Promotion of Science (JSPS).Awais, Muhammad et al. | 2006
- 2779
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Generating Isotropic Superparamagnetic Interconnectivity for the Two‐Dimensional Organization of Nanostructured Building BlocksChen, Hao Ming / Liu, Ru‐Shi / Li, Hongliang / Zeng, Hua Chun et al. | 2006
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Generating Isotropic Superparamagnetic Interconnectivity for the Two-Dimensional Organization of Nanostructured Building Blocks. The authors gratefully acknowledge the financial support of the Ministry of Education, Singapore.Chen, Hao Ming et al. | 2006
- 2783
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Flattened Cone 2,8,14,20-Tetrakis(L-valinamido)[4]resorcinarene: An Enantioselective Allosteric Receptor in the Gas Phase. This work was supported by the Ministero dell'Istruzione dell'Università e della Ricerca (MIUR, COFIN), the Consiglio Nazionale delle Ricerche (CNR), and the Istituto Pasteur Fondazione Cenci Bolognetti. B.B. and A.T. gratefully acknowledge Project "FIRB 2003" from MIUR (Ministero della Università e della Ricerca). We are grateful to F. Angelelli for technical assistance.Botta, Bruno et al. | 2006
- 2783
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Flattened Cone 2,8,14,20‐Tetrakis(L‐valinamido)[4]resorcinarene: An Enantioselective Allosteric Receptor in the Gas PhaseBotta, Bruno / Caporuscio, Fabiana / Subissati, Deborah / Tafi, Andrea / Botta, Maurizio / Filippi, Antonello / Speranza, Maurizio et al. | 2006
- 2786
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Room‐Temperature Nucleophilic Aromatic Fluorination: Experimental and Theoretical StudiesSun, Haoran / DiMagno, Stephen G. et al. | 2006
- 2786
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Room-Temperature Nucleophilic Aromatic Fluorination: Experimental and Theoretical Studies. We thank the Nebraska Research Initiative for financial support of this research, Rieke Metals Inc. for the gift of the substrates, and the Research Computing Facility at the University of Nebraska for supercomputer time.Sun, Haoran et al. | 2006
- 2791
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Construction of a Ball-and-Spike Protein Supramolecule. We are grateful to T. Douglas for a gift of the LisDps clone. A part of this work was supported by the Nanotechnology Support Project of the Ministry of Education, Culture, Sports, Science, and Technology (MEXT), Japan, at the Research Center for Ultrahigh Voltage Electron Microscopy, Osaka University.Sugimoto, Kenji et al. | 2006
- 2791
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Construction of a Ball‐and‐Spike Protein SupramoleculeSugimoto, Kenji / Kanamaru, Shuji / Iwasaki, Kenji / Arisaka, Fumio / Yamashita, Ichiro et al. | 2006
- 2794
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A Genetically Encoded Photocaged TyrosineDeiters, Alexander / Groff, Dan / Ryu, Youngha / Xie, Jianming / Schultz, Peter G. et al. | 2006
- 2794
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A Genetically Encoded Photocaged Tyrosine. A.D. gratefully acknowledges a postdoctoral fellowship from the Deutsche Forschungsgemeinschaft. This work was supported by funding from the National Institutes of Health (GM62159) and the Department of Energy (ER46051). This is manuscript 17952-CH of The Scripps Research Institute.Deiters, Alexander et al. | 2006
- 2797
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Total Synthesis of (+)-b-ErythroidineFukumoto, H. / Takahashi, K. / Ishihara, J. / Hatakeyama, S. et al. | 2006
- 2797
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Total Synthesis of (+)-b-Erythroidine. This work was partly supported by a Grant-in-Aid for Scientific Research on Priority Areas (16073213) from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT). We thank Prof. Takanori Suzuki (Graduate School of Science, Hokkaido University) for the X-ray analysis of 16.Fukumoto, Hironori et al. | 2006
- 2797
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Total Synthesis of (+)‐β‐ErythroidineFukumoto, Hironori / Takahashi, Keisuke / Ishihara, Jun / Hatakeyama, Susumi et al. | 2006
- 2800
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Rh-Catalyzed [4+2] Annulation of 4-Alkynals with Isocyanates and Its Application to the Parallel Kinetic Resolution of Unfunctionalized 4-Alkynals. We thank Takasago International Corporation for the gift of segphos and Prof. Gregory C. Fu (Massachusetts Institute of Technology, USA) for his helpful encouragement.Tanaka, Ken et al. | 2006
- 2800
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Rh‐Catalyzed [4+2] Annulation of 4‐Alkynals with Isocyanates and Its Application to the Parallel Kinetic Resolution of Unfunctionalized 4‐AlkynalsTanaka, Ken / Hagiwara, Yuji / Hirano, Masao et al. | 2006
- 2803
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Oxidative De‐aromatization of para‐Alkyl Phenols into para‐Peroxyquinols and para‐Quinols Mediated by Oxone as a Source of Singlet OxygenCarreño, M. Carmen / González‐López, Marcos / Urbano, Antonio et al. | 2006
- 2803
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Oxidative De-aromatization of para-Alkyl Phenols into para-Peroxyquinols and para-Quinols Mediated by Oxone as a Source of Singlet Oxygen. We thank the Ministerio de Ciencia y Tecnologia (Grants BQU2002-03371 and CTQ2005-02095-BQU) and the Comunidad Autonoma de Madrid (Grant GR-MAT-0152-2004) for financial support. M.G.-L. thanks the Comunidad Autonoma de Madrid for a fellowship.Carreño, M.Carmen et al. | 2006
- 2807
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Hydrosilylation of Alkenes with Early Main-Group Metal Catalysts. We kindly acknowledge H. Bandmann, Dr. T. Schaller, and W. Karow for measurement of the NMR (500 MHz) spectra, GCMS analyses, and many fruitful discussions.Buch, Frank et al. | 2006
- 2807
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Hydrosilylation of Alkenes with Early Main‐Group Metal CatalystsBuch, Frank / Brettar, Julie / Harder, Sjoerd et al. | 2006
- 2811
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Polymethacrylates with a Covalently Linked CuII-Cyclen Complex for the In Situ Generation of Nitric Oxide from Nitrosothiols in Blood. We thank the NIH (EB-000783 and EB-004527) for the financial support of this research.Hwang, Sangyeul et al. | 2006
- 2811
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Polymethacrylates with a Covalently Linked CuII–Cyclen Complex for the In Situ Generation of Nitric Oxide from Nitrosothiols in BloodHwang, Sangyeul / Cha, Wansik / Meyerhoff, Mark. E. et al. | 2006
- 2814
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Substrate Specificity of the Macrolide-Glycosylating Enzyme Pair DesVII-DesVIII: Opportunities, Limitations, and Mechanistic Hypotheses. This work was supported in part by the National Institutes of Health (grants GM35906 and GM54346 (H.-w.L.) and AI52218, CA84374 and GM70637) and an NCDDG grant (U19 CA113297) from the National Cancer Institute (J.S.T.).Borisova, Svetlana A. et al. | 2006
- 2814
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Substrate Specificity of the Macrolide‐Glycosylating Enzyme Pair DesVII/DesVIII: Opportunities, Limitations, and Mechanistic HypothesesBorisova, Svetlana A. / Zhang, Changsheng / Takahashi, Haruko / Zhang, Hua / Wong, Alexander W. / Thorson, Jon S. / Liu, Hung‐wen et al. | 2006
- 2819
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Reactivity‐Based One‐Pot Synthesis of the Tumor‐Associated Antigen N3 Minor Octasaccharide for the Development of a Photocleavable DIOS‐MS Sugar ArrayLee, Jinq‐Chyi / Wu, Chung‐Yi / Apon, Junefredo V. / Siuzdak, Gary / Wong, Chi‐Huey et al. | 2006
- 2819
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Reactivity-Based One-Pot Synthesis of the Tumor-Associated Antigen N3 Minor Octasaccharide for the Development of a Photocleavable DIOS-MS Sugar Array. J.-C.L. and C.-Y.W. contributed equally. This work was supported by the NIH. C.-Y.W. thanks the National Science Council of Taiwan and the Genomics Research Center, Academia Sinica for financial support. DIOS-MS=desorption-ionization on silicon mass spectrometry.Lee, Jinq-Chyi et al. | 2006
- 2824
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Short Oxo-Titanium(IV) Bond in Bacterial Transferrin: A Protein Target for Metalloantibiotics. We thank the Wellcome Trust, Overseas Research Student Award, and University of Massachusetts Dartmouth for their support for this work.Guo, Maolin et al. | 2006
- 2824
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Short Oxo–Titanium(IV) Bond in Bacterial Transferrin: A Protein Target for MetalloantibioticsGuo, Maolin / Harvey, Ian / Campopiano, Dominic J. / Sadler, Peter J. et al. | 2006
- 2827
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Catalysis in Capillaries by Pd Thin Films Using Microwave‐Assisted Continuous‐Flow Organic Synthesis (MACOS)Shore, Gjergji / Morin, Sylvie / Organ, Michael G. et al. | 2006
- 2827
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Catalysis in Capillaries by Pd Thin Films Using Microwave-Assisted Continuous-Flow Organic Synthesis (MACOS). This work was funded by the Ontario Research and Development Challenge Fund (ORDCF), Canada Foundation for Innovation (CFI), the Ontario Innovation Trust (OIT), NSERC, and York University. The authors are grateful to Biotage Inc. for the donation of a Smith Creator Synthesizer to develop this new methodology. We acknowledge Ross Davidson at Surface Science Western, University of Western Ontario, London, ON, for the SEM and EDX measurements.Shore, Gjergji et al. | 2006
- 2832
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Rhenium‐ and Aniline‐Catalyzed One‐Pot Annulation of Aromatic Ketones and α,β‐Unsaturated Esters Initiated by CH Bond ActivationKuninobu, Yoichiro / Nishina, Yuta / Shouho, Makoto / Takai, Kazuhiko et al. | 2006
- 2832
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Rhenium- and Aniline-Catalyzed One-Pot Annulation of Aromatic Ketones and [alpha],b-Unsaturated Esters Initiated by CH Bond Activation. Financial support by a Grant-in-Aid for Scientific Research on Priority Areas (No. 14078219, "Reaction Control of Dynamic Complexes") from the Ministry of Education, Culture, Sports, Science, and Technology of Japan.Kuninobu, Yoichiro et al. | 2006
- 2832
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Rhenium- and Aniline-Catalyzed One-Pot Annulation of Aromatic Ketones and a,b-Unsaturated Esters Initiated by C H Bond ActivationKuninobu, Y. / Nishina, Y. / Shouho, M. / Takai, K. et al. | 2006
- 2835
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Total Syntheses of Hexacyclinol, 5‐epi‐Hexacyclinol, and Desoxohexacyclinol Unveil an Antimalarial Prodrug MotifLa Clair, James J. et al. | 2006
- 2835
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Total Syntheses of Hexacyclinol, 5-epi-Hexacyclinol, and Desoxohexacyclinol Unveil an Antimalarial Prodrug Motif. A considerable portion of this work was conducted during 1999-2002 at Bionic Bros GmbH, Germany. J.J.L.C. acknowledges the assistance of five technicians.La Clair, James J. et al. | 2006
- 2839
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Cyclic Dimethylsiloxanes as Pseudo Crown Ethers: Syntheses and Characterization of Li(Me2SiO)5[Al{OC(CF3)3}4], Li(Me2SiO)6[Al{OC(CF3)3}4], and Li(Me2SiO)6[Al{OC(CF3)2Ph}4]Decken, Andreas / Passmore, Jack / Wang, Xinping et al. | 2006
- 2839
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Cyclic Dimethylsiloxanes as Pseudo Crown Ethers: Syntheses and Characterization of Li(Me2SiO)5[Al{OC(CF3)3}4], Li(Me2SiO)6[Al{OC(CF3)3}4], and Li(Me2SiO)6[Al{OC(CF3)2Ph}4]. Acknowledgement is made to NSERC (Canada) for financial support of this research, Mikko Rautiainen for help with calculations, and Dr. Carsten Knapp for his helpful suggestions.Decken, Andreas et al. | 2006
- 2844
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An Organic Photoelectrode Working in the Water Phase: Visible‐Light‐Induced Dioxygen Evolution by a Perylene Derivative/Cobalt Phthalocyanine BilayerAbe, Toshiyuki / Nagai, Keiji / Kabutomori, Satoko / Kaneko, Masao / Tajiri, Akio / Norimatsu, Takayoshi et al. | 2006
- 2844
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An Organic Photoelectrode Working in the Water Phase: Visible-Light-Induced Dioxygen Evolution by a Perylene Derivative-Cobalt Phthalocyanine Bilayer. This work was partially supported by Grant-in-Aid for Scientific Research (No. 15750110 (T.A.)) and for Scientific Research in Priority Areas (Fundamental Science and Technology of Photofunctional Interfaces, No. 417 (T.A., K.N., and M.K.)) from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT), Japan.Abe, Toshiyuki et al. | 2006
- 2848
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Highly Active, Productive, and Syndiospecific Yttrium Initiators for the Polymerization of Racemic b-ButyrolactoneAmgoune, A. / Thomas, C. M. / Ilinca, S. / Roisnel, T. / Carpentier, J. F. et al. | 2006
- 2848
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Highly Active, Productive, and Syndiospecific Yttrium Initiators for the Polymerization of Racemic b-Butyrolactone. This research was financially supported in part by the Region Bretagne (grant-in-aid COPOBIO to A.A.). We thank A. Bondon (University of Rennes 1) for NMR experiments.Amgoune, Abderramane et al. | 2006
- 2848
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Highly Active, Productive, and Syndiospecific Yttrium Initiators for the Polymerization of Racemic β‐ButyrolactoneAmgoune, Abderramane / Thomas, Christophe M. / Ilinca, Simona / Roisnel, Thierry / Carpentier, Jean‐François et al. | 2006
- 2848
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Highly active, productive, and syndiospecific yttrium initiators for the polymerization of racemic beta-butyrolactoneAmgoune, Abderramane / Thomas, Christophe M. / Ilinca, Simona / Roisnel, Thierry / Carpentier, Jean-Francois et al. | 2006
- 2851
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Highly Enantioselective Conjugate Reduction of b,b-Disubstituted [alpha],b-Unsaturated Nitriles. This work was supported by a Korea Research Foundation grant funded by the Korean Government (R08-2004-000-10429-0). The LC and GC equipment was supported by the Faculty Research Fund 2005, Sungkyunkwan University. Prof. C. Song and E. Kwon at SKKU are acknowledged for valuable advice and assistance with the chiral analysis.Lee, Daehyung et al. | 2006
- 2851
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Highly enantioselective conjugate reduction of beta,beta-disubstituted alpha,beta-unsaturated nitrilesLee, Daehyung / Kim, Daesung / Yun, Jaesook et al. | 2006
- 2851
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Highly Enantioselective Conjugate Reduction of b,b-Disubstituted a,b-Unsaturated NitrilesLee, D. / Kim, D. / Yun, J. et al. | 2006
- 2851
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Highly Enantioselective Conjugate Reduction of β,β‐Disubstituted α,β‐Unsaturated NitrilesLee, Daehyung / Kim, Daesung / Yun, Jaesook et al. | 2006
- 2855
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Ligandenbibliotheken fur die hocheffiziente Rhodium-Phosphoramidit-katalysierte asymmetrische Arylierung von N,N-Dimethylsulfamoyl-geschutzten AldiminenJagt, R. B. / Toullec, P. Y. / Geerdink, D. / de Vries, J. G. / Feringa, B. L. / Minnaard, A. J. et al. | 2006
- 2855
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Ligandenbibliotheken für die hocheffiziente Rhodium‐Phosphoramidit‐katalysierte asymmetrische Arylierung von N,N‐Dimethylsulfamoyl‐geschützten AldiminenJagt, Richard B. C. / Toullec, Patrick Y. / Geerdink, Danny / de Vries, Johannes G. / Feringa, Ben L. / Minnaard, Adriaan J. et al. | 2006
- 2855
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Ligandenbibliotheken für die hocheffiziente Rhodium-Phosphoramidit-katalysierte asymmetrische Arylierung von N,N-Dimethylsulfamoyl-geschützten Aldiminen. Wir danken der Firma DSM, dem niederländischen Wirtschaftsministerium und der Dutch Science Foundation NWO-CW für die finanzielle Unterstützung im Rahmen des CW-Combichem-Programms. Herrn E. P. Schudde und Frau T. D. Tiemersma-Wegman danken wir für die technische Unterstützung.Jagt, Richard B.C. et al. | 2006
- 2858
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Die Struktur eines neunkernigen Gallium(III)-hydroxid-Clusters - eine Zwischenstufe bei der Bildung eines zweikernigen dreistrangigen Helicats?Albrecht, M. / Dehn, S. / Frohlich, R. et al. | 2006
- 2858
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Die Struktur eines neunkernigen Gallium(III)-hydroxid-Clusters - eine Zwischenstufe bei der Bildung eines zweikernigen dreisträngigen Helicats?. Diese Arbeit wurde von der Deutschen Forschungsgemeinschaft unterstützt (GK 440 "Methoden der asymmetrischen Synthese").Albrecht, Markus et al. | 2006
- 2858
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Die Struktur eines neunkernigen Gallium(III)‐hydroxid‐Clusters – eine Zwischenstufe bei der Bildung eines zweikernigen dreisträngigen Helicats?Albrecht, Markus / Dehn, Sabrina / Fröhlich, Roland et al. | 2006
- 2860
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Ein sechskerniges Eisen(III)-carboxylat mit [Fe6(µ3-O)3(µ2-OH)]11+-Kernstruktur als effizienter Katalysator zur Oxidation von Cycloalkanen. Diese Arbeit wurde durch DSM Fine Chemicals Austria und die Universität Wien finanziell unterstützt. Wir danken B. Mienert (Max-Planck-Institut für Bioanorganische Chemie, Mülheim a. d. Ruhr) für die Aufnahme der Mößbauer-Spektren. Prof. Ya. D. Lampeka, Dr. S. Shova und N. A. Sheddan danken wir für wertvolle Diskussionen.Trettenhahn, Günter et al. | 2006
- 2860
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Ein sechskerniges Eisen(III)-carboxylat mit [Fe6(m3-O)3(m2-OH)]11+-Kernstruktur als effizienter Katalysator zur Oxidation von CycloalkanenTrettenhahn, G. / Nagl, M. / Neuwirth, N. / Arion, V. B. / Jary, W. / Pochlauer, P. / Schmid, W. et al. | 2006
- 2860
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Ein sechskerniges Eisen(III)‐carboxylat mit [Fe6(μ3‐O)3(μ2‐OH)]11+‐Kernstruktur als effizienter Katalysator zur Oxidation von CycloalkanenTrettenhahn, Günter / Nagl, Michael / Neuwirth, Norbert / Arion, Vladimir B. / Jary, Walther / Pöchlauer, Peter / Schmid, Walther et al. | 2006
- 2865
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Spaltung der N2‐Dreifachbindung durch Ti2: ein Weg zu molekularen Materialien für die N2‐Aktivierung?Himmel, Hans‐Jörg / Hübner, Olaf / Klopper, Wim / Manceron, Laurent et al. | 2006
- 2865
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Spaltung der N2-Dreifachbindung durch Ti2: ein Weg zu molekularen Materialien für die N2-Aktivierung?. H.-J.H. dankt für finanzielle Unterstützung durch die DFG und den DAAD (PROCOPE-Stipendium). W.K. dankt für die Unterstützung durch die DFG im Rahmen des Zentrums für funktionelle Nanostrukturen (CFN, Projekt-Nr. C3.3). L.M. dankt für Unterstützung durch das Centre National de la Recherche Scientifique (PICS3032) und das Ministère des Affaires Etrangères (PROCOPE09643SG).Himmel, Hans-Jörg et al. | 2006
- 2865
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Spaltung der N2-Dreifachbindung durch Ti2: ein Weg zu molekularen Materialien fur die N2-Aktivierung?Himmel, H. J. / Hubner, O. / Klopper, W. / Manceron, L. et al. | 2006
- 2869
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Strukturelle und spektroskopische Charakterisierung von lichtemittierenden NatriumlanthanoidtetrafluoridenAebischer, Annina / Hostettler, Marc / Hauser, Jürg / Krämer, Karl / Weber, Thomas / Güdel, Hans Ulrich / Bürgi, Hans‐Beat et al. | 2006
- 2869
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Strukturelle und spektroskopische Charakterisierung von lichtemittierenden Natriumlanthanoidtetrafluoriden. Wir danken Prof. R. B. Neder für seine Hilfe beim Einsatz seines Programmpakets DISCUS und D. Biner für Mithilfe bei den Synthesen. Diese Arbeit wurde durch den Schweizerischen Nationalfonds zur Förderung der wissenschaftlichen Forschung finanziell unterstützt.Aebischer, Annina et al. | 2006
- 2879
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Vorschau: Angew. Chem. 17/2006| 2006