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Titelbild: 3‐Boryl‐2,2′‐bithiophene as a Versatile Core Skeleton for Full‐Color Highly Emissive Organic Solids (Angew. Chem. 23/2007)
Die Berechnung relativer Energien mit approximativer Dichtefunktionaltheorie - eine WarnungFNR HREF="nss"> FN ID="nss"> Diese Arbeit wurde von der Justus-Liebig-Universität Gießen unterstützt. Ich danke Stefan Grimme, Donald Truhlar und Paul von R. Schleyer für hilfreiche Diskussionen und Matthew D. Wodrich für die Daten in Abbildung FIGR HREF="fig1">1.
Amplification and Transcription of the Dynamic Supramolecular Chirality of the Guanine QuadruplexFNR HREF="nss"> FN ID="nss"> This work, conducted as part of the award "Dynamic Adaptative Materials for Separation and Sensing Microsystems" made under the European Heads of Research Councils and European Science Foundation EURYI (European Young Investigator) Awards Scheme in 2004, was supported by funds from the Participating Organisations of EURYI and the EC Sixth Framework Programme. See URL XML-LINK="SIMPLE" HREF="http: www.esf.org-euryi">http: www.esf.org-euryi.
3-Boryl-2,2'-bithiophene as a Versatile Core Skeleton for Full-Color Highly Emissive Organic SolidsFNR HREF="nss"> FN ID="nss"> This work was partially supported by SORST, JST, and the TOYOTA Motor Co.
δ Aromaticity in [Ta3O3]-FNR HREF="nss"> FN ID="nss"> The theoretical work done at Utah was supported by the donors of the Petroleum Research Fund, administered by the American Chemical Society and the National Science Foundation. The experimental work done at Washington was supported by the Chemical Sciences, Geosciences, and Biosciences Division, Office of Basic Energy Sciences, U.S. Department of Energy (DOE) under the catalysis center program and was performed at the EMSL, a national scientific user facility sponsored by the DOE's Office of Biological and Environmental Research and located at Pacific Northwest National Laboratory, operated for the DOE by Battelle.
Inducing and Sensing Protein-Protein Interactions in Living Cells by Selective Cross-linkingFNR HREF="nss"> FN ID="nss"> This work was supported by the Swiss National Science Foundation, the Human Frontier Science Program, and the Boehringer-Ingelheim Foundation. We thank Thomas Gronemeyer for technical assistance and Nils Johnsson, Helen O'Hare, and Arnaud Gautier for discussions.
A Supramolecular-Hydrogel-Encapsulated Hemin as an Artificial Enzyme to Mimic PeroxidaseFNR HREF="nss"> FN ID="nss"> This work was partially supported by RGC of Hong Kong (HKU2-05C, 604905, 600504) and EHIA (HKUST).
Photochemical Activation of Protein Expression in Bacterial CellsFNR HREF="nss"> FN ID="nss"> D.D.Y. thanks the US Department of Education for a GAANN Biotechnology Fellowship. This research was supported in part by research grant no. 5-FY05-1215 from the March of Dimes Birth Defects Foundation.
Selective Adsorption and Separation of Xylene Isomers and Ethylbenzene with the Microporous Vanadium(IV) Terephthalate MIL-47FNR HREF="nss"> FN ID="nss"> L.A. and J.D. are grateful to F.W.O.-Vlaanderen (Research Foundation-Flanders) for positions as a research assistant and post-doctoral researcher, respectively. This work was performed in the frame of the IAP Functional Supramolecular Systems of the Belgian Federal Government.
Metal Oxide "Nanosponges" as Chemical Sensors: Highly Sensitive Detection of Hydrogen with Nanosponge TitaniaFNR HREF="nss"> FN ID="nss"> We acknowledge financial support of this work from the Microsystems Technology Office of the Defence Advanced Research Projects Agency. This work made use of UCSB MRL Central Facilities supported by MRSEC Program of the NSF under Award No. DMR-00-8034. A.S.Z. is grateful to the Agency for Science, Technology and Research (A*STAR, Singapore) for the award of an International Fellowship (National Science Scholars Program).
[(dpp-bian)Zn&bond;Zn(dpp-bian)]: A Zinc-Zinc-Bonded Compound Supported by Radical-Anionic LigandsFNR HREF="nss"> FN ID="nss"> This work was supported by the Alexander von Humboldt Foundation (I.L.F. and S.Y.K.) and the Russian Foundation for Basic Research (grant no. 07-03-00545); dpp-bian=1,2-bis[(2,6-diisopropylphenyl)imino]acenaphth- ene.
Highly Stable Pyrimidine-Motif Triplex Formation at Physiological pH Values by a Bridged Nucleic Acid AnalogueFNR HREF="nss"> FN ID="nss"> S.M.A.R. thanks the Japan Society of Promotion of Science (JSPS) for financial support.
In Situ Time-Resolved Dynamic Surface Events on the Pt-C Cathode in a Fuel Cell under Operando ConditionsFNR HREF="nss"> FN ID="nss"> This work has been performed with the approval of SPring-8 (Proposal No. 2005A0451-NXa-np) and PF PAC (Proposal No. 2005G207).
A Pocket-Sized Convective PCR ThermocyclerFNR HREF="nss"> FN ID="nss"> This work was supported by the National Institutes of Health under grants K22-HG02297 and R01-HG003364. We thank Prof. Mihir Sen for helpful discussions regarding modeling the convective flow. We are also grateful to Ling Zhen for assistance with computational-flow simulations.
DNA Binding and Catalytic Properties of Positively Charged CorrolesFNR HREF="nss"> FN ID="nss"> This work was supported by the German Israel Cooperation (Z.G.) and by the Israel Science Foundation under Grants No. 254-04 (I.G.) and 330-04 (Z.G.).
Polymorphic Superelasticity in Semicrystalline PolymersFNR HREF="nss"> FN ID="nss"> Financial support from the "Ministero dell'Istruzione, dell'Università e della Ricerca" (PRIN 2004 project) is gratefully acknowledged. The time-resolved X-ray data were obtained at the CCLRC Synchrotron Radiation Source at Daresbury (UK).
A Magnetic-Nanoparticle-Supported 4-N,N-Dialkylaminopyridine Catalyst: Excellent Reactivity Combined with Facile Catalyst Recovery and RecyclabilityFNR HREF="nss"> FN ID="nss"> Financial support from the Irish Research Council for Science Engineering and Technology, Science Foundation Ireland, and Trinity College Dublin is gratefully acknowledged.
Hexasilylated Total Carbomer of BenzeneFNR HREF="nss"> FN ID="nss"> Synthesis of Ring Carbomers, Part VI. This research was supported by the Centre National de la Recherche Scientifique and by the Ministère de l'Enseignement Supérieur de la Recherche et de la Technologie (ACI funding). - Parts I-V: refs. BIBR HREF="bib2b">2b, BIBR HREF="bib9a">9a, BIBR HREF="bib9b">b, BIBR HREF="bib5a">5a, BIBR HREF="bib5b">b.
Superparamagnetic Magnetite Colloidal Nanocrystal ClustersFNR HREF="nss"> FN ID="nss"> Y.Y. thanks the University of California, Riverside for startup funds. We thank Dr. J. Guo and Dr. C. Dong at the Lawrence Berkeley National Laboratory for help with the XAS analyses, and Dr. K. N. Bozhilov and Mr. S. McDaniel at the Central Facility for Advanced Microscopy and Microanalysis at UCR for assistance with the TEM measurements.
Quantum Dot-Bioluminescence Resonance Energy Transfer Based Highly Sensitive Detection of ProteasesFNR HREF="nss"> FN ID="nss"> This work was supported by the Department of Defense Breast Cancer Research Program Concept Award and the National Cancer Institute Centers of Cancer Nanotechnology Excellence (1U54A119367-01). Y.Z. was supported partially by the Stanford School of Medicine Dean's Fellowship.
Total Synthesis of the Potent Antitumor Macrolides Pladienolide B and DFNR HREF="nss"> FN ID="nss"> We are grateful to Dr. T. Tsuchida (Mercian Corp.) for supplying the natural products. We thank T. Uehara, M. Gotoda, S. Naito, and M. Gomibuchi for performing compound analyses; A. Okuda for purifying compounds by HPLC; as well as T. Sakai and Dr. Y. Fukuda for their help. We thank Dr. T. Owa, Dr. D. Rossignol, and Dr. R. Lebedev for proof-reading the manuscript.
Amino Acid Phosphoramidate Nucleotides as Alternative Substrates for HIV-1 Reverse TranscriptaseFNR HREF="nss"> FN ID="nss"> This work was supported by funding under the Sixth Research Framework Programme of the European Union, Project RIGHT (LSHB-CT-2004-005276). We thank Dr. Natalia Duybankova for assistance in NMR assignment and analysis.
Total Synthesis of (-)-Ulapualide A: The Danger of Overdependence on NMR Spectroscopy in Assignment of StereochemistryFNR HREF="nss"> FN ID="nss"> We thank J. Kempson for his contributions to the synthesis of intermediate 11. We also thank Astra Zeneca and Pfizer Ltd for financial support towards this research program.
Iron-Catalyzed Alkylations of Aromatic Grignard ReagentsFNR HREF="nss"> FN ID="nss"> We thank the CNRS and the Ecole Supérieure de Chimie Organique et Minérale (ESCOM) for their financial support as well as the Ministère de l'Education Nationale et de la Recherche for its financial support and a grant to A.M. The Fondation de France is acknowledged for a grant to C.D. and V.H.
Enantioselective Synthesis of Protected Amines by the Catalytic Asymmetric Addition of Hydrazoic Acid to KetenesFNR HREF="nss"> FN ID="nss"> Support has been provided by the National Institutes of Health (National Institute of General Medical Sciences: R01-GM57034), Merck Research Laboratories, and Novartis. We thank Dr. P. Mueller and L. Firmansjah for X-ray analysis.
Integration of a Self-Assembling Protein Scaffold with Water-Soluble Single-Walled Carbon NanotubesFNR HREF="nss"> FN ID="nss"> We gratefully acknowledge the Biomolecular Materials Program at LBNL and the UCB Chemical Biology Graduate Program for generous financial support. We also thank A. Paul Alivisatos for the use of his AFM.
Dinuclear Ruthenium(II) Triple-Stranded Helicates: Luminescent Supramolecular Cylinders That Bind and Coil DNA and Exhibit Activity against Cancer Cell LinesFNR HREF="nss"> FN ID="nss"> We thank the University of Birmingham and the ORS Scheme (G.P.) for support, the EU for a Marie Curie fellowship (A.H.; MEIF-CT-2005-024818) and Professor Kevin Chipman (Birmingham) for access to cell-line testing facilities.
Dinuclear Ruthenium(II) Triple‐Stranded Helicates: Luminescent Supramolecular Cylinders That Bind and Coil DNA and Exhibit Activity against Cancer Cell Lines
Pascu, Gabriel I.
/ Hotze, Anna C. G.
/ Sanchez‐Cano, Carloset al.
| 2007
Highly Selective Thiiranation of 1,2-Allenyl Sulfones with Br2 and Na2S2O3: Mechanism and Asymmetric Synthesis of AlkylidenethiiranesFNR HREF="nss"> FN ID="nss"> We gratefully acknowledge the National Natural Science Foundation of China (No. 20572093), the Zhejiang Provincial Natural Science Foundation of China (Y 404262), and the Cheung Kong Scholar Program for financial support. We thank Zhan Lu in our group for reproducing the results presented in entries 2 and 11 of Table 2 and entry 1 of Table 3. S.M. is appointed jointly by Zhejiang University and Shanghai Institute of Organic Chemistry. This research was conducted at Zhejiang University.
Polyamid-Stützen für DNA-ArchitekturenFNR HREF="nss"> FN ID="nss"> Diese Arbeit wurde durch Drittmittel für A.H. und M.F. ermöglicht (SFB 624, "Template - Vom Design chemischer Schablonen zur Reaktionssteuerung"). Die großzügige Förderung der DFG für A.H. im Rahmen des Emmy-Noether-Programmes sei dankend erwähnt. Bei Frau Dr. Marion Ritzi bedanken wir uns für hilfreiche Diskussionen.
UEQN LOC="INLINE" NOTAT="TEX">{{{\hfill 3\atop \hfill \infty }}}[Eu(Tzpy)2], ein homoleptisches Raumnetz mit ikosaedrischer Stickstoffkoordination von EuIIFNR HREF="nss"> FN ID="nss"> Diese Arbeit wurde von der Deutschen Forschungsgemeinschaft im Rahmen des SPP1166 "Lanthanoid-spezifische Funktionalitäten" gefördert. Wir danken Prof. Dr. G. Meyer für seine Unterstützung. Tzpy-=C5H4N4-.
Vernetzbare Lochleiter für blau phosphoreszierende organische LeuchtdiodenFNR HREF="nss"> FN ID="nss"> Diese Arbeit wurde vom Bundesministerium für Bildung und Forschung (BMBF) unterstützt. Wir danken Dr. Jürgen Steiger (Degussa, Marl) für die UPS-Daten und Georgios Liaptsis (Universität zu Köln) für seine Hilfe bei der Synthese.
Die supramolekulare Struktur von 5 nm großen sphärischen Micellen mit D3-Symmetrie, selbstorganisiert aus einem amphiphilen [3:3]-Hexakisaddukt von C60FNR HREF="nss"> FN ID="nss"> Wir danken der Deutschen Forschungsgemeinschaft für großzügige finanzielle Unterstützung von A.H. (DFG AH468-13-1) und C.B. (DFG BO1000-6-1).
Die supramolekulare Struktur von 5 nm großen sphärischen Micellen mit D3‐Symmetrie, selbstorganisiert aus einem amphiphilen [3:3]‐Hexakisaddukt von C60
Schade, Boris
/ Ludwig, Kai
/ Böttcher, Christophet al.
| 2007
C2-symmetrische Metacyclophane - eine mögliche Alternative zu o,o'-verbrückten BinaphthylenFNR HREF="nss"> FN ID="nss"> Der Autor dankt der Deutschen Forschungsgemeinschaft (DFG) für die finanzielle Unterstützung. Dr. Andreea Schuster, Dr. Rolf Roers und Dipl.-Ing. Heinz Bandmann möchte ich für die vielen hilfreichen Diskussion danken.