المؤلفون: Stahlberger, Mareen, Schwarz, Noah, Zippel, Christoph, Hohmann, Jens, Nieger, Martin, Hassan, Zahid, Brase, Stefan

المساهمون: Department of Chemistry

مصطلحات موضوعية: Fused-imidazoles, Groebke-Blackburn-Bienayme (GBB) reaction, Isocyanide Chemistry, Multicomponent reactions, [2, 2]Paracyclophane, PALLADACYCLE, ISOCYANIDE, EFFICIENT, DERIVATIVES, RESOLUTION, PYRAZINES, 116 Chemical sciences

وصف الملف: application/pdf

العلاقة: The authors acknowledge Deutsche Forschungsgemeinschaft (DFG) support under Germany's Excellence Strategy - 3DMM2O - EXC-2082/1-390761711, the KIT Campus Transfer GmbH for the financial support to MS for her Ph.D. studies. We thank the technical and analytical staff at IOC (KIT) for assistance. Open Access funding enabled and organized by Projekt DEAL.; Stahlberger , M , Schwarz , N , Zippel , C , Hohmann , J , Nieger , M , Hassan , Z & Brase , S 2022 , ' Diversity-Oriented Synthesis of [2.2]Paracyclophane-derived Fused Imidazo[1,2-a]heterocycles by Groebke-Blackburn-Bienayme Reaction : Accessing Cyclophanyl Imidazole Ligands Library ' , Chemistry: A European Journal , vol. 28 , no. 3 , e202103511 . https://doi.org/10.1002/chem.202103511Test; ORCID: /0000-0003-1677-0109/work/108461765; 52c49971-d9ab-42ab-ad93-e9c0a07b2284; http://hdl.handle.net/10138/340569Test; 000728131500001

الإتاحة: http://hdl.handle.net/10138/340569Test

المؤلفون: Wei Gong (112494), Haomiao Xie (4053265), Karam B. Idrees (8636154), Florencia A. Son (8690583), Zhijie Chen (1610659), Fanrui Sha (9515622), Yan Liu (25061), Yong Cui (318757), Omar K. Farha (1301625)

مصطلحات موضوعية: Biochemistry, Medicine, Ecology, Cancer, Space Science, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, three carboxylate linkers, new 2d net, heat pump regulation, gathered significant interest, distinct topological structures, 88 g g, 72 g g, scu , flu , fcu , high uptake capacities, 40 – 60, 2 ]­ paracyclophane, 6 , , water sorption, water adsorption, two tetratopic, trifluoroacetic acid, steep pore, reticular design, reticular construction, reticular chemistry

العلاقة: https://figshare.com/articles/journal_contribution/Water_Sorption_Evolution_Enabled_by_Reticular_Construction_of_Zirconium_Metal_Organic_Frameworks_Based_on_a_Unique_2_2_Paracyclophane_Scaffold/18864083Test

الإتاحة: https://doi.org/10.1021/jacs.1c11836.s001Test

المؤلفون: Zippel, Christoph, Israil, Roumany, Schüssler, Lars, Hassan, Zahid, Schneider, Erik K., Weis, Patrick, Nieger, Martin, Bizzarri, Claudia, Kappes, Manfred M., Riehn, Christoph, Diller, Rolf, Braese, Stefan

المساهمون: Department of Chemistry

مصطلحات موضوعية: metal-to-metal distance modulation, heterometallic complexes, cooperative effects, photoredox catalysis, [2, 2]paracyclophane, gold, ruthenium, ELECTROORGANIC CHEMISTRY, PHOTOPHYSICAL PROPERTIES, RUTHENIUM(II) COMPLEXES, PLANAR, LIGAND, BOND, PHOTOCHEMISTRY, REARRANGEMENT, DERIVATIVES, POTENTIALS, 116 Chemical sciences

وصف الملف: application/pdf

العلاقة: This work is supported by the DFG-funded Collaborative Research Centre (SFB) TRR 88/3MET "Cooperative Effects in Homo-and Heterometallic Complexes" at Karlsruhe Institute of Technology (KIT) and TU Kaiserslautern. ZH and SB acknowledge Deutsche Forschungsgemeinschaft (DFG) under Germany's Excellence Strategy 3DMM2O-EXC-2082/1-390761711 for financial contributions. CR and RI are thankful for financial support by the DFG Priority Program SPP 2102 "Light-controlled reactivity of metal complexes". Open Access funding enabled and organized by Projekt DEAL.; Zippel , C , Israil , R , Schüssler , L , Hassan , Z , Schneider , E K , Weis , P , Nieger , M , Bizzarri , C , Kappes , M M , Riehn , C , Diller , R & Braese , S 2021 , ' Metal-to-Metal Distance Modulated Au(I)/Ru(II) Cyclophanyl Complexes : Cooperative Effects in Photoredox Catalysis ' , Chemistry: A European Journal , vol. 27 , no. 61 , pp. 15187-15200 . https://doi.org/10.1002/chem.202102341Test; ORCID: /0000-0003-1677-0109/work/104150895; b6f6a541-0380-4899-9074-470f974cc3f9; http://hdl.handle.net/10138/337035Test; 000711934000001

الإتاحة: http://hdl.handle.net/10138/337035Test

المؤلفون: Zippel, Christoph, Bartholomeyzik, Teresa, Friedmann, Christian, Nieger, Martin, Hassan, Zahid, Brase, Stefan

المساهمون: Department of Chemistry

مصطلحات موضوعية: Cyclometallation, Palladacycles, Planar chirality, [2, 2]Paracyclophane, Regioselectivity, PALLADACYCLE, COMPLEXES, EFFICIENT, LIGANDS, 116 Chemical sciences

وصف الملف: application/pdf

العلاقة: Zippel , C , Bartholomeyzik , T , Friedmann , C , Nieger , M , Hassan , Z & Brase , S 2021 , ' Regioselective ortho-Palladation of [2.2]Paracyclophane Scaffolds : Accessing Planar and Central Chiral N,C-Palladacycles ' , European Journal of Organic Chemistry , vol. 2021 , no. 36 , pp. 5090-5093 . https://doi.org/10.1002/ejoc.202101066Test; ORCID: /0000-0003-1677-0109/work/101133778; eba74887-5a40-48c1-ad14-3f2dfef27812; http://hdl.handle.net/10138/335026Test; 000701324300010

الإتاحة: http://hdl.handle.net/10138/335026Test

المؤلفون: Dan Xu (138152), Wen-Hua Zheng (64486)

مصطلحات موضوعية: Biochemistry, Molecular Biology, Physiology, Developmental Biology, Mental Health, Plant Biology, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, synthesized using palladium, planar chiral heteroarenes, planar chiral azahelicene, paracyclophane three pairs, optically pure 4, mediated oxidative cyclization, 2 ]­ paracyclophane, remarkably stronger, hypervalent iodine, chiroptical properties

العلاقة: https://figshare.com/articles/journal_contribution/Synthesis_and_Chiroptical_Properties_of_Planar_Chiral_Azahelicenes_Based_on_2_2_Paracyclophane/16810905Test

الإتاحة: https://doi.org/10.1021/acs.orglett.1c03325.s001Test

المؤلفون: Kang Li (107509), Honghan Ji (11656493), Zeren Yang (11656496), Wenzeng Duan (1991755), Yudao Ma (1672645), Houting Liu (2492929), Huaiwei Wang (6582332), Shuwen Gong (11656499)

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Cell Biology, Genetics, Molecular Biology, Biotechnology, Sociology, Plant Biology, Space Science, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, rationalized via x, moderate quantum yields, highly demanded due, 3d boranil complexes, 2 ]­ paracyclophane, small organic cpl, complexes display aggregation, 2 , work describes, solid state, ray diffraction, r <, promising applications, photophysical properties, new family, n ̂, dft calculations, chiroptical devices

العلاقة: https://figshare.com/articles/journal_contribution/3D_Boranil_Complexes_with_Aggregation-Amplified_Circularly_Polarized_Luminescence/16943996Test

الإتاحة: https://doi.org/10.1021/acs.joc.1c01956.s001Test

المؤلفون: Shiqi Wu (3913507), Laura Abad Galán (9582993), Margaux Roux (11553296), François Riobé (1962967), Boris Le Guennic (7162721), Yannick Guyot (1593238), Tangui Le Bahers (8694927), Laurent Micouin (1710223), Olivier Maury (1593244), Erica Benedetti (1950958)

مصطلحات موضوعية: Biophysics, Biochemistry, Plant Biology, Chemical Sciences not elsewhere classified, triazacyclonane macrocyclic ligand, theoretical study reveals, ensure efficient sensitization, space paracyclophane conjugation, resulting complexes eu, gd ­( iii, 2 ]­ paracyclophane, singlet oxygen generation, singlet oxygen, tuning excited, state properties, multistep synthesis, lanthanide ions, fully emissive, conjugated skeleton, complex acts, combined photophysical

العلاقة: https://figshare.com/articles/journal_contribution/Tuning_Excited-State_Properties_of_2_2_Paracyclophane-Based_Antennas_to_Ensure_Efficient_Sensitization_of_Lanthanide_Ions_or_Singlet_Oxygen_Generation/16799483Test

الإتاحة: https://doi.org/10.1021/acs.inorgchem.1c01986.s001Test

المؤلفون: Zippel, Christoph, Spuling, Eduard, Hassan, Zahid, Polamo, Mika, Nieger, Martin, Bräse, Stefan

المساهمون: Department of Chemistry

مصطلحات موضوعية: [2, 2]paracyclophane, aryl-aryl coupling, Buchwald-Hartwig amination, C-H activation, cyclophanes, palladium, FUNCTIONALIZATION, PARACYCLOPHANES, POLYMERIZATION, LIGAND, 116 Chemical sciences

وصف الملف: application/pdf

العلاقة: This work is supported by the Helmholtz Association Program at the Karlsruhe Institute of Technology. The authors acknowledge support from Deutsche Forschungsgemeinschaft under Germany's Excellence Strategy -3DMM2O-EXC-2082/1-390761711. Open access funding enabled and organized by Projekt DEAL.; Zippel , C , Spuling , E , Hassan , Z , Polamo , M , Nieger , M & Bräse , S 2020 , ' Controlling Regioselectivity in Palladium-Catalyzed C-H Activation/Aryl-Aryl Coupling of 4-Phenylamino[2.2]paracyclophane ' , Chemistry: A European Journal , vol. 26 , no. 61 , pp. 13771-13775 . https://doi.org/10.1002/chem.202003709Test; ORCID: /0000-0003-1677-0109/work/85116749; fce719b4-b1fa-4768-8150-00ccd13f15c6; http://hdl.handle.net/10138/322822Test; 000570192200001

الإتاحة: http://hdl.handle.net/10138/322822Test

المؤلفون: Knoll, Daniel M., Hu, Yuling, Hassan, Zahid, Nieger, Martin, Bräse, Stefan

المساهمون: Department of Chemistry

مصطلحات موضوعية: [2, 2]paracyclophane ligands, N-H insertion, alpha-diazocarbonyls, planar chirality, copper catalysis, ASYMMETRIC CONJUGATE ADDITION, ENANTIOSELECTIVE INSERTION, BONDS, CATALYSTS, DESIGN, IMINES, 116 Chemical sciences

وصف الملف: application/pdf

العلاقة: This research was funded by SBF/TRR88 3MET (B2).; Knoll , D M , Hu , Y , Hassan , Z , Nieger , M & Bräse , S 2019 , ' Planar Chiral [2.2]Paracyclophane-Based Bisoxazoline Ligands and Their Applications in Cu-Mediated N-H Insertion Reaction ' , Molecules , vol. 24 , no. 22 . https://doi.org/10.3390/molecules24224122Test; ORCID: /0000-0003-1677-0109/work/67131489; 3ae12f84-4bad-43e7-87c1-426b670ec70c; http://hdl.handle.net/10138/309137Test; 000501529700111

الإتاحة: http://hdl.handle.net/10138/309137Test

المؤلفون: Zippel, Christoph, Hassan, Zahid, Nieger, Martin, Bräse, Stefan

المساهمون: Department of Chemistry

مصطلحات موضوعية: Catalyst Design, Bimetallic Catalysts, Chiral dirhodium(II) complexes, Cyclopropanation, Planar Chirality, [2, 2]Paracyclophane, C-H FUNCTIONALIZATION, INTERMOLECULAR REACTIONS, ENANTIOSELECTIVE CYCLOPROPENATION, INSERTION REACTIONS, ORGANIC-SYNTHESIS, YLIDE GENERATION, DIAZOESTERS, COMPLEXES, TETRACARBOXYLATES, DERIVATIVES, 116 Chemical sciences

وصف الملف: application/pdf

العلاقة: This research has been funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under Germany's Excellence Strategy - 2082/1-390761711. The authors acknowledge generous support for this research by the Karlsruhe Institute of Technology (KIT) and the DFG-funded Collaborative Research Centre (SFB) TRR 88/3MET "Cooperative Effects in Homo-and Heterometallic Complexes" is gratefully acknowledged.; Zippel , C , Hassan , Z , Nieger , M & Bräse , S 2020 , ' Design and Synthesis of a [2.2]Paracyclophane-based Planar Chiral Dirhodium Catalyst and its Applications in Cyclopropanation Reaction of Vinylarenes with alpha-Methyl-alpha-Diazo Esters ' , Advanced Synthesis & Catalysis , vol. 362 , no. 16 , pp. 3431-3436 . https://doi.org/10.1002/adsc.202000512Test; ORCID: /0000-0003-1677-0109/work/79516867; 33c831a2-107c-43d9-8e44-33126e5fb4c8; http://hdl.handle.net/10138/318494Test; 000548181100001

الإتاحة: http://hdl.handle.net/10138/318494Test