Titelbild: Toroidal Micelles of Uniform Size from Diblock Copolymers (Angew. Chem. 25/2009) (German)
- New search for: Huang, Haiying
- New search for: Chung, Bonghoon
- New search for: Jung, Jueun
- New search for: Park, Hae‐Woong
- New search for: Chang, Taihyun
- New search for: Huang, Haiying
- New search for: Chung, Bonghoon
- New search for: Jung, Jueun
- New search for: Park, Hae‐Woong
- New search for: Chang, Taihyun
In:
Angewandte Chemie
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121
, 25
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4519
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2009
- Article (Journal) / Electronic Resource
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Title:Titelbild: Toroidal Micelles of Uniform Size from Diblock Copolymers (Angew. Chem. 25/2009)
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Contributors:Huang, Haiying ( author ) / Chung, Bonghoon ( author ) / Jung, Jueun ( author ) / Park, Hae‐Woong ( author ) / Chang, Taihyun ( author )
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Published in:Angewandte Chemie ; 121, 25 ; 4519
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Publisher:
- New search for: WILEY‐VCH Verlag
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Publication date:2009-06-08
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Size:2 pages
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:German
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Keywords:
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Source:
Table of contents – Volume 121, Issue 25
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 4519
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Titelbild: Toroidal Micelles of Uniform Size from Diblock Copolymers (Angew. Chem. 25/2009)Huang, Haiying / Chung, Bonghoon / Jung, Jueun / Park, Hae‐Woong / Chang, Taihyun et al. | 2009
- 4520
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Innentitelbild: Multicompartmental Microcylinders (Angew. Chem. 25/2009)Bhaskar, Srijanani / Hitt, Jonathon / Chang, Sei‐Won Laura / Lahann, Joerg et al. | 2009
- 4523
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Graphisches Inhaltsverzeichnis: Angew. Chem. 25/2009| 2009
- 4535
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Iridium‐Catalyzed Reactions of Trifluoromethylated Compounds with Alkenes: A CH Bond Activation α to the Trifluoromethyl GroupGuo, Yong / Zhao, Xiaming / Zhang, Dazhi / Murahashi, Shun‐Ichi et al. | 2009
- 4535
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Iridium-Catalyzed Reactions of Trifluoromethylated Compounds with Alkenes: A Csp3 H Bond Activation a to the Trifluoromethyl GroupGuo, Y. / Zhao, X. / Zhang, D. / Murahashi, S. I. et al. | 2009
- 4535
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Iridium-Catalyzed Reactions of Trifluoromethylated Compounds with Alkenes: A Csp3&bond;H Bond Activation α to the Trifluoromethyl Group This work was supported by Grants-in-aid for Scientific Research, Ministry of Education, Culture, Sports, Science and Technology of Japan.Guo, Yong et al. | 2009
- 4538
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Top-Beitrage aus unseren Schwesterzeitschriften: Angew. Chem. 25/2009| 2009
- 4538
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Top‐Beiträge aus unseren Schwesterzeitschriften: Angew. Chem. 25/2009| 2009
- 4540
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Wenbin Lin| 2009
- 4541
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Nanochemie: Mirkin ausgezeichnet / Biochemie: Shokat geehrt / Theorie: Warshel gewählt| 2009
- 4541
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Nanochemie: Mirkin ausgezeichnet / Biochemie: Shokat geehrt / Theorie: Warshel gewahlt| 2009
- 4542
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Microemulsions.Background, New Concepts, Applications, Perspectives. Herausgegeben von Cosima Stubenrauch.Walsh, Dominic et al. | 2009
- 4544
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Ist die Enantioselektivität bei der asymmetrischen Katalyse vorhersagbar?Brown, John M. / Deeth, Robert J. et al. | 2009
- 4544
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Ist die Enantioselektivität bei der asymmetrischen Katalyse vorhersagbar? Wir danken der Leverhulme Foundation für ein Stipendium (J.M.B.) und Prof. R. W. Alder (Bristol) für wertvolle kritische Anmerkungen.Brown, John M et al. | 2009
- 4544
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Ist die Enantioselektivitat bei der asymmetrischen Katalyse vorhersagbar?Brown, J. M. / Deeth, R. J. et al. | 2009
- 4548
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Koordinationsgesteuerte Selbstorganisation von PEO‐funktionalisierten Perylenbisimiden – supramolekulare Vielfalt bei Verwendung weniger molekularer BausteineGebers, Jan / Rolland, Damien / Frauenrath, Holger et al. | 2009
- 4548
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Koordinationsgesteuerte Selbstorganisation von PEO-funktionalisierten Perylenbisimiden - supramolekulare Vielfalt bei Verwendung weniger molekularer Bausteine Wir danken für Unterstützung durch den Fonds der Chemischen Industrie (Chemiefonds-Stipendium für Jan Gebers) und die Materials for the Life Sciences Unit des Swiss Competence Centre for Materials Research and Technology of the ETH Domain. PEO: Polyethylenoxid.Gebers, Jan et al. | 2009
- 4552
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Enzymkatalyse “in neuem Licht”Gärtner, Wolfgang et al. | 2009
- 4556
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Miniemulsionspolymerisation und Struktur von Polymer- und Hybridnanopartikeln Veröffentlicht zum 25. Gründungsjubiläum des Max-Planck-Instituts für Polymerforschung, Mainz.Landfester, Katharina et al. | 2009
- 4556
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Miniemulsionspolymerisation und Struktur von Polymer‐ und HybridnanopartikelnLandfester, Katharina et al. | 2009
- 4578
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A Supramolecularly Assisted Transformation of Block-Copolymer Micelles into Nanotubes The authors acknowledge support from the NSF Center for Polymer Interfaces and Macromolecular Assemblies (CPIMA: NSF-DMR-0213618). We thank Timothy Yeow and Andy Ong in FEI (Japan) for TEM support.Kim, Sung Ho et al. | 2009
- 4578
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A Supramolecularly Assisted Transformation of Block‐Copolymer Micelles into NanotubesKim, Sung Ho / Nederberg, Fredrik / Jakobs, Robert / Tan, Jeremy P. K. / Fukushima, Kazuki / Nelson, Alshakim / Meijer, E. W. / Yang, Yi Yan / Hedrick, James L. et al. | 2009
- 4583
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CH Hydroxylation Using a Heterocyclic Catalyst and Aqueous H2O2Litvinas, Nichole D. / Brodsky, Benjamin H. / Du Bois, J. et al. | 2009
- 4583
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C&bond;H Hydroxylation Using a Heterocyclic Catalyst and Aqueous H2O2 We thank Prof. John Brauman for helpful discussions and A. Sloan Devlin for preparing and performing intial test reactions with the substrate appearing in entry 6 of Table 2. N.D.L. gratefully acknowledges the National Science Foundation and Novartis for predoctoral fellowships. We thank Pfizer, Inc. for support of this work.Litvinas, Nichole D et al. | 2009
- 4587
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Addition of Dimethylaminobismuth to Aldehydes, Ketones, Alkenes, and AlkynesNekoueishahraki, Bijan / Sarish, Sankaranarayana Pillai / Roesky, Herbert W. / Stern, Daniel / Schulzke, Carola / Stalke, Dietmar et al. | 2009
- 4587
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Addition of Dimethylaminobismuth to Aldehydes, Ketones, Alkenes, and Alkynes Support of the Deutsche Forschungsgemeinschaft is highly acknowledged.Nekoueishahraki, Bijan et al. | 2009
- 4591
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A Unified Strategy for Exceptionally High Diastereoselectivity in the Photochemical Ring Closure of Chiral DiarylethenesYokoyama, Yasushi / Shiozawa, Tatsuya / Tani, Yutaka / Ubukata, Takashi et al. | 2009
- 4591
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A Unified Strategy for Exceptionally High Diastereoselectivity in the Photochemical Ring Closure of Chiral Diarylethenes This work was supported by a Grant-in-Aid for Scientific Research on Priority Areas (471) "Photochromism" from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT) of the Japanese Government.Yokoyama, Yasushi et al. | 2009
- 4594
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Efficient Replication Bypass of Size-Expanded DNA Base Pairs in Bacterial Cells We thank the U.S. National Institutes of Health (CA80024 to J.M.E. and GM63587 to E.T.K.) for support. J.G. and H.L. acknowledge Stanford Graduate Fellowships.Delaney, James C et al. | 2009
- 4594
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Efficient Replication Bypass of Size‐Expanded DNA Base Pairs in Bacterial CellsDelaney, James C. / Gao, Jianmin / Liu, Haibo / Shrivastav, Nidhi / Essigmann, John M. / Kool, Eric T. et al. | 2009
- 4598
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Palladium‐Catalyzed Cyanation of CarbonCarbon Triple Bonds Under Aerobic ConditionsArai, Shigeru / Sato, Takashi / Koike, Yuka / Hayashi, Michino / Nishida, Atsushi et al. | 2009
- 4598
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Palladium-Catalyzed Cyanation of Carbon&bond;Carbon Triple Bonds Under Aerobic Conditions We thank Professors Motohiro Akazome and Shinji Harada (Chiba University) for their kind support with the X-ray crystallographic analysis. S.A. thanks the Inohana Foundation (Chiba University) for financial support.Arai, Shigeru et al. | 2009
- 4602
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N‐Heterocyclic Carbene Gold(I) Catalyzed Transformation of N‐Tethered 1,5‐Bisallenes to 6,7‐Dimethylene‐3‐azabicyclo[3.1.1]heptanesKim, Soo Min / Park, Ji Hoon / Kang, Youn Kyung / Chung, Young Keun et al. | 2009
- 4602
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N-Heterocyclic Carbene Gold(I) Catalyzed Transformation of N-Tethered 1,5-Bisallenes to 6,7-Dimethylene-3-azabicyclo[3.1.1]heptanes This work was supported by the Korean Government (MOEHRD) (KRF-2008-341-C00022), and the SRC-ERC program of MOST-KOSEF (R11-2005-065). J.H.P. acknowledges support of the Brain Korea 21 fellowships and S.M.K. acknowledges the receipt of the Brain Korea 21 fellowships and a Seoul Science Fellowship.Kim, Soo Min et al. | 2009
- 4606
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Low‐Temperature Atomic Layer Deposition of Copper Metal Thin Films: Self‐Limiting Surface Reaction of Copper Dimethylamino‐2‐propoxide with DiethylzincLee, Byoung H. / Hwang, Jae K. / Nam, Jae W. / Lee, Song U. / Kim, Jun T. / Koo, Sang‐M. / Baunemann, A. / Fischer, Roland A. / Sung, Myung M. et al. | 2009
- 4606
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Low-Temperature Atomic Layer Deposition of Copper Metal Thin Films: Self-Limiting Surface Reaction of Copper Dimethylamino-2-propoxide with Diethylzinc This work was supported by a Korea Science and Engineering Foundation (KOSEF) grant funded by the Korea government (MOST) (No. 2008-02378), the SRC-ERC program of MOST-KOSEF (grant R11-2005-048-00000-0), a Korea Research Foundation Grant funded by the Korea government (MOEHRD, Basic Research Promotion Fund) (KRF-2007-313-C00383), and the Priority Program "Anorganische Materialien durch Gasphasensynthese" (SPP 1119) of the Deutsche Forschungsgemeinschaft.Lee, Byoung H et al. | 2009
- 4610
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Laser‐Modulated Ordering of Gold Nanoparticles at the Air/Water InterfaceVolinsky, Roman / Jelinek, Raz et al. | 2009
- 4613
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Nickel‐Catalyzed Formation of a Carbon–Nitrogen Bond at the β Position of Saturated KetonesUeno, Satoshi / Shimizu, Ryosuke / Kuwano, Ryoichi et al. | 2009
- 4613
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Nickel-Catalyzed Formation of a Carbon-Nitrogen Bond at the β Position of Saturated Ketones This work was supported by the Global-COE program "Science of Future Molecular Systems". We acknowledge Prof. Tsutomu Katsuki for GCMS analyses.Ueno, Satoshi et al. | 2009
- 4613
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Nickel-Catalyzed Formation of a Carbon-Nitrogen Bond at the b Position of Saturated KetonesUeno, S. / Shimizu, R. / Kuwano, R. et al. | 2009
- 4616
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Indirect Optical Analysis of a Dynamic Chemical SystemGasparini, Giulio / Bettin, Federico / Scrimin, Paolo / Prins, Leonard J. et al. | 2009
- 4616
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Indirect Optical Analysis of a Dynamic Chemical System We acknowledge financial support from the University of Padova (CPDA054893) and MIUR (PRIN2006).Gasparini, Giulio et al. | 2009
- 4621
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Facile Dissociation of [(LNiII)2E2] Dichalcogenides: Evidence for [LNiIIE2] Superselenides and Supertellurides in SolutionYao, Shenglai / Xiong, Yun / Zhang, Xinhao / Schlangen, Maria / Schwarz, Helmut / Milsmann, Carsten / Driess, Matthias et al. | 2009
- 4621
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Facile Dissociation of [(LNiII)2E2] Dichalcogenides: Evidence for [LNiIIE2] Superselenides and Supertellurides in Solution Financial support from the Cluster of Excellence "Unifying Concepts in Catalysis" (EXC 314-1) funded by the Deutsche Forschungsgemeinschaft and administered by the Technische Universität Berlin is gratefully acknowledged. We sincerely thank Prof. Dr. K. Wieghardt for helpful discussions, Dr. E. Bill for magnetic measurements and Dr. T. Weyhermüller (Max Planck Institute for Bioinorganic Chemistry, Mülheim)) for crystallographic measurements. X.Z. is grateful to the Alexander von Humboldt Stiftung for a postdoctoral fellowship. L=β-diketiminate; E=Se, Te.Yao, Shenglai et al. | 2009
- 4625
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Self-Mediated Stereoselective Oxidation of Thia-Capped Cyclodextrins We thank the Agence Nationale de la Recherche for support (ANR Watercat).Armspach, Dominique et al. | 2009
- 4625
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Self‐Mediated Stereoselective Oxidation of Thia‐Capped CyclodextrinsArmspach, Dominique / Matt, Dominique / Toupet, Loic et al. | 2009
- 4629
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Phosphonium Salts as Chiral Phase‐Transfer Catalysts: Asymmetric Michael and Mannich Reactions of 3‐AryloxindolesHe, Rongjun / Ding, Changhua / Maruoka, Keiji et al. | 2009
- 4629
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Phosphonium Salts as Chiral Phase-Transfer Catalysts: Asymmetric Michael and Mannich Reactions of 3-Aryloxindoles This work was supported by a Grant-in-Aid for Scientific Research on the Priority Area "Advanced Molecular Transformation of Carbon Resources" from the Ministry of Education, Culture, Sports, Science and Technology (Japan).He, Rongjun et al. | 2009
- 4632
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Self‐Healing Colloidal CrystalsIyer, Ashlee St. John / Lyon, L. Andrew et al. | 2009
- 4632
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Self-Healing Colloidal Crystals The authors thank Zhiyong Meng for providing the pNIPAm-AAc microgels and Profs. Victor Breedveld and Alberto Fernandez-Nieves for many valuable discussions. L.A.L. acknowledges support from the ACS-PRF.Iyer, Ashlee St John et al. | 2009
- 4637
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Oxidative Carbocation Formation in Macrocycles: Synthesis of the Neopeltolide MacrocycleTu, Wangyang / Floreancig, Paul E. et al. | 2009
- 4637
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Oxidative Carbocation Formation in Macrocycles: Synthesis of the Neopeltolide Macrocycle We thank the National Institutes of Health (GM062924) and the National Science Foundation (CHE-139851) for generous support of this research, and the NIH for the 700 MHz NMR instrument at the University of Pittsburgh (S10RR023404). We thank Dr. Steve Geib for crystallographic analysis.Tu, Wangyang et al. | 2009
- 4642
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Indoles from Simple Anilines and Alkynes: Palladium‐Catalyzed CH Activation Using Dioxygen as the OxidantShi, Zhuangzhi / Zhang, Chun / Li, Si / Pan, Delin / Ding, Shengtao / Cui, Yuxin / Jiao, Ning et al. | 2009
- 4642
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Indoles from Simple Anilines and Alkynes: Palladium-Catalyzed C&bond;H Activation Using Dioxygen as the Oxidant Financial support from Peking University, the National Science Foundation of China (Nos. 20702002, 20872003), and the National Basic Research Program of China (973 Program 2009CB825300) are greatly appreciated.Shi, Zhuangzhi et al. | 2009
- 4647
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Regio‐ and Stereoselective Generation of Alkenylindium Compounds from Indium Tribromide, Alkynes, and Ketene Silyl AcetalsNishimoto, Yoshihiro / Moritoh, Ryosuke / Yasuda, Makoto / Baba, Akio et al. | 2009
- 4647
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Regio- and Stereoselective Generation of Alkenylindium Compounds from Indium Tribromide, Alkynes, and Ketene Silyl Acetals This work was supported by a Grant-in-Aid for Scientific Research on Priority Areas (grant no. 18065015, "Chemistry of Concerto Catalysis" and grant no. 20036036, "Synergistic Effects for Creation of Functional Molecules") and for Scientific Research (grant no. 19550038) from the Ministry of Education, Culture, Sports, Science and Technology (Japan). We thank Dr. Nobuko Kanehisa for the valuable advice regarding X-ray crystallography. Y. N. thanks The Global COE Program "Global Education and Research Center for Bio-Environment Chemistry" of Osaka University.Nishimoto, Yoshihiro et al. | 2009
- 4651
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Fast Attrition‐Enhanced Deracemization of Naproxen by a Gradual In Situ FeedNoorduin, Wim L. / Kaptein, Bernard / Meekes, Hugo / van Enckevort, Willem J. P. / Kellogg, Richard M. / Vlieg, Elias et al. | 2009
- 4651
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Fast Attrition-Enhanced Deracemization of Naproxen by a Gradual In Situ Feed The SNN agency (Cooperation Northern Netherlands) and the European Fund for Regional Development (EFRO) are acknowledged for partial financial support of this work.Noorduin, Wim L et al. | 2009
- 4654
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9,10‐Dihydro‐9,10‐diboraanthracene: Supramolecular Structure and Use as a Building Block for Luminescent Conjugated PolymersLorbach, Andreas / Bolte, Michael / Li, Haiyan / Lerner, Hans‐Wolfram / Holthausen, Max C. / Jäkle, Frieder / Wagner, Matthias et al. | 2009
- 4654
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9,10-Dihydro-9,10-diboraanthracene: Supramolecular Structure and Use as a Building Block for Luminescent Conjugated Polymers A.L. thanks the Fonds der Chemischen Industrie for a Ph.D. grant. F.J. thanks the NSF (CHE-0809642) and the Alexander von Humboldt Foundation for a Friedrich Wilhelm Bessel Research Award. This work was supported by the Deutsche Forschungsgemeinschaft, the Chemetall GmbH, and the City Solar AG, Bad Kreuznach.Lorbach, Andreas et al. | 2009
- 4659
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Multicompartmental MicrocylindersBhaskar, Srijanani / Hitt, Jonathon / Chang, Sei‐Won Laura / Lahann, Joerg et al. | 2009
- 4659
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Multicompartmental Microcylinders Published on the occasion of the 25th anniversary of the Max Planck Institute for Polymer Research, Mainz. We thank Dr. Xuwei Jiang, University of Michigan, for synthesizing the acetylene-functionalized PLGA, Chris Edwards, Microscopy and Image Analysis Lab, University of Michigan, for guidance in cryosectioning, and Prof. David C. Martin, University of Michigan for valuable discussions. J.L. gratefully acknowledges financial support from the Department of Defense (Idea Award, W81XWH-06-1-0271).Bhaskar, Srijanani et al. | 2009
- 4664
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Toroidal Micelles of Uniform Size from Diblock Copolymers Published on the occasion of the 25th anniversary of the Max Planck Institute for Polymer Research, Mainz. This work was supported by NRL (R0A-2007-000-20125-0), SRC (R11-2008-052-03002-0), and WCU (R31-2008-000-10059-0) programs.Huang, Haiying et al. | 2009
- 4664
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Toroidal Micelles of Uniform Size from Diblock CopolymersHuang, Haiying / Chung, Bonghoon / Jung, Jueun / Park, Hae‐Woong / Chang, Taihyun et al. | 2009
- 4668
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An Aqueous Route to Multicolor Photoluminescent Carbon Dots Using Silica Spheres as CarriersLiu, Ruili / Wu, Dongqing / Liu, Shuhua / Koynov, Kaloian / Knoll, Wolfgang / Li, Qin et al. | 2009
- 4668
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An Aqueous Route to Multicolor Photoluminescent Carbon Dots Using Silica Spheres as Carriers Published on the occasion of the 25th anniversary of the Max Planck Institute for Polymer Research, Mainz. We thank Dr. Y. Zhang for the AFM characterization, K. Kirchhoff for the TEM characterization, and Prof. N. Heckenberg for the helpful discussions. R.L. and S.L. acknowledge Alexander von Humboldt (AvH) Fellowships. S.L. also thanks Singapore Millennium Foundation (SMF) for financial support. Q.L. is grateful to Dr. E.-K. Sinner's Bio-lab at the Max Planck Institute for Polymer Research for hosting, the technical assistance from M. Droege, E. Conrad, and A. Arslan, and the partial support from Australian Research Council under DP0558727.Liu, Ruili et al. | 2009
- 4672
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Subliming the Unsublimable: How to Deposit Nanographenes This work was financially supported by the DFG project OPTOELEKTRONIK (MU 334-28-1; AOBJ: 539724), and the EU project NAIMO (NMP-CT-2004-500355).Rouhanipour, Ali et al. | 2009
- 4672
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Subliming the Unsublimable: How to Deposit NanographenesRouhanipour, Ali / Roy, Mainak / Feng, Xinliang / Räder, Hans Joachim / Müllen, Klaus et al. | 2009
- 4675
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Asymmetric Hydroxylative Phenol Dearomatization through In Situ Generation of Iodanes from Chiral Iodoarenes and m‐CPBAQuideau, Stéphane / Lyvinec, Gildas / Marguerit, Mélanie / Bathany, Katell / Ozanne‐Beaudenon, Aurélie / Buffeteau, Thierry / Cavagnat, Dominique / Chénedé, Alain et al. | 2009
- 4675
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Asymmetric Hydroxylative Phenol Dearomatization through In Situ Generation of Iodanes from Chiral Iodoarenes and m-CPBA We thank Simafex, the Association Nationale de la Recherche Technique (CIFRE Grants No. 457-2005 & 301-2002), and the Institut Universitaire de France for their financial support. m-CPBA=meta-chloroperoxybenzoic acid.Quideau, Stéphane et al. | 2009
- 4680
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Hyperbranched: A Universal Conjugated Polymer Platform Published on the occasion of the 25th anniversary of the Max Planck Institute for Polymer Research, Mainz. We thank the Department of Energy-Basic Energy Sciences (DE-FG02-04ER46141)for generous financial support. J.T. thanks Junta de Comunidades de Castilla La Mancha (Fondo Social Europeo FSE 2007-2013) for his postdoctoral grant.Tolosa, Juan et al. | 2009
- 4680
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Hyperbranched: A Universal Conjugated Polymer PlatformTolosa, Juan / Kub, Chris / Bunz, Uwe H. F. et al. | 2009
- 4683
-
Spontaneous Formation of Giant Unilamellar Vesicles from Microdroplets of a Polyion Complex by Thermally Induced Phase SeparationOana, Hidehiro / Kishimura, Akihiro / Yonehara, Kei / Yamasaki, Yuichi / Washizu, Masao / Kataoka, Kazunori et al. | 2009
- 4683
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Spontaneous Formation of Giant Unilamellar Vesicles from Microdroplets of a Polyion Complex by Thermally Induced Phase Separation We are grateful to Dr. S. Fukuda (the University of Tokyo Hospital) for his valuable help with the TEM measurements. This research was supported in part by KAKENHI (no. 19031003, no. 20034008) from MEXT, JAPAN. A.K. thanks the Inoue Foundation for Science, the Izumi Science and Technology, and the Kao Foundation for Arts and Sciences.Oana, Hidehiro et al. | 2009
- 4687
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Local and Collective Motions in Precise Polyolefins with Alkyl Branches: A Combination of 2H and 13C Solid-State NMR Spectroscopy Published on the occasion of the 25th anniversary of the Max Planck Institute for Polymer Research, Mainz. Support by the National Science Foundation under grant DMR-0703261, and by the International Max Planck Research School for Polymer Materials, Mainz is greatly acknowledged. We also thank Dr. Giovanni Rojas for kindly providing the ADMET PE sample.Wei, Yuying et al. | 2009
- 4687
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Local and Collective Motions in Precise Polyolefins with Alkyl Branches: A Combination of 2H and 13C Solid‐State NMR SpectroscopyWei, Yuying / Graf, Robert / Sworen, John C. / Cheng, Chi‐Yuan / Bowers, Clifford R. / Wagener, Kenneth B. / Spiess, Hans Wolfgang et al. | 2009
- 4691
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Kooperative Molekulbewegungen innerhalb eines selbstorganisierten flussigkristallinen molekularen Drahtes am Beispiel eines TEG- substituierten PerylendiimidsHansen, M. R. / Schnitzler, T. / Pisula, W. / Graf, R. / Mullen, K. / Spiess, H. W. et al. | 2009
- 4691
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Kooperative Molekülbewegungen innerhalb eines selbstorganisierten flüssigkristallinen molekularen Drahtes am Beispiel eines TEG- substituierten Perylendiimids Veröffentlicht zum 25. Gründungsjubiläum des Max-Planck-Instituts für Polymerforschung, Mainz. M.R.H. dankt der Carlsberg Stiftung für ein Forschungsstipendium. Wir danken Dr. Daniel Sebastiani für die quantenchemische Berechnung von 13C-NMR-chemischen Verschiebungen. TEG=Triethylenglycol.Hansen, Michael Ryan et al. | 2009
- 4691
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Kooperative Molekülbewegungen innerhalb eines selbstorganisierten flüssigkristallinen molekularen Drahtes am Beispiel eines TEG‐ substituierten PerylendiimidsHansen, Michael Ryan / Schnitzler, Tobias / Pisula, Wojciech / Graf, Robert / Müllen, Klaus / Spiess, Hans Wolfgang et al. | 2009
- 4696
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Fingerabdrucke von DNA-Polymerasen: mehrfache simultane Enzym-Charakterisierung auf DNA-ArraysKranaster, R. / Marx, A. et al. | 2009
- 4696
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Fingerabdrücke von DNA-Polymerasen: mehrfache simultane Enzym-Charakterisierung auf DNA-Arrays Wir danken der DFG (SPP1170) und dem BMBF (BioChancePlus) für finanzielle Unterstützung.Kranaster, Ramon et al. | 2009
- 4696
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Fingerabdrücke von DNA‐Polymerasen: mehrfache simultane Enzym‐Charakterisierung auf DNA‐ArraysKranaster, Ramon / Marx, Andreas et al. | 2009
- 4700
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Kontrollierte Oligomerisierung von Lewis-Säure-Base-stabilisierten Phosphanylalanen Diese Arbeit wurde durch die Deutsche Forschungsgemeinschaft und den Fonds der Chemischen Industrie unterstützt.Bodensteiner, Michael et al. | 2009
- 4700
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Kontrollierte Oligomerisierung von Lewis-Saure/Base-stabilisierten PhosphanylalanenBodensteiner, M. / Vogel, U. / Timoshkin, A. Y. / Scheer, M. et al. | 2009
- 4700
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Kontrollierte Oligomerisierung von Lewis‐Säure/Base‐stabilisierten PhosphanylalanenBodensteiner, Michael / Vogel, Ulf / Timoshkin, Alexey Y. / Scheer, Manfred et al. | 2009
- 4705
-
Enantiospezifische Synthese und Allylierung ausschlielich Kohlenstoff-substituierter, a-chiraler AllylstannaneSchmidtmann, E. S. / Oestreich, M. et al. | 2009
- 4705
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Enantiospezifische Synthese und Allylierung ausschließlich Kohlenstoff‐substituierter, α‐chiraler AllylstannaneSchmidtmann, Eric S. / Oestreich, Martin et al. | 2009
- 4705
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Enantiospezifische Synthese und Allylierung ausschließlich Kohlenstoff-substituierter, α-chiraler Allylstannane Wir danken der Deutschen Forschungsgemeinschaft (Oe 249-3-1) für finanzielle Unterstützung und der BASF AG (Ludwigshafen) für die großzügige Bereitstellung von Enzymen. M.O. dankt der Aventis Foundation für ein Karl-Winnacker-Stipendium (2006-2008).Schmidtmann, Eric S et al. | 2009
- 4710
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Lithiumdotierung eines hydroxymodifizierten MIL-53-Strukturanalogons zur Verbesserung der Wasserstoffadsorption Dieses Projekt wurde von der Universität Augsburg sowie von General Motors Fuel Cell Activities unterstützt. Besonderer Dank gilt Dr. Ulrich Eberle (GM Fuel Cell Activities) für interessante Diskussionen und Anregungen zum Thema Wasserstoff- und Brennstoffzellentechnologie für Automobilanwendungen.Himsl, Dieter et al. | 2009
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Lithiumdotierung eines hydroxymodifizierten MIL‐53‐Strukturanalogons zur Verbesserung der WasserstoffadsorptionHimsl, Dieter / Wallacher, Dirk / Hartmann, Martin et al. | 2009
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Hydroaminierung eines Alkens, induziert durch niederenergetische Elektronen P.S. dankt Sven Doye für einen inspirierenden GDCh-Vortrag über Hydroaminierungen. Diese Arbeit wurde durch die DFG und das COST-Programm ECCL gefördert.Hamann, Thorben et al. | 2009
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Hydroaminierung eines Alkens, induziert durch niederenergetische ElektronenHamann, Thorben / Böhler, Esther / Swiderek, Petra et al. | 2009
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Nomenklatur der Rotaxane und PseudorotaxaneSchomburg, Ida et al. | 2009
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Nomenklatur der Rotaxane und Pseudorotaxane Copyright© der englischen Fassung, die unter dem Titel "Nomenclature for Rotaxanes and Pseudorotaxanes" von A. Yerin (Moskau) für die Veröffentlichung in Pure Appl. Chem. 2008, 80, 2041-2068BIBR HREF="bib27">27 vorbereitet wurde: International Union of Pure and Applied Chemistry, 2008. - Wir danken der IUPAC für die Genehmigung zum Druck einer deutschen Fassung dieser Recommendation.Schomburg, Ida et al. | 2009
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Vorschau: Angew. Chem. 26/2009| 2009