TY - JOUR A1 - Abdalla, Hassan E. A1 - Abramowski, Attila A1 - Aharonian, Felix A. A1 - Benkhali, Faiçal Ait A1 - Akhperjanian, A. G. A1 - Angüner, Ekrem Oǧuzhan A1 - Arrieta, M. A1 - Aubert, Pierre A1 - Backes, Michael A1 - Balzer, Arnim A1 - Barnard, Michelle A1 - Becherini, Yvonne A1 - Tjus, Julia Becker A1 - Berge, David A1 - Bernhard, Sabrina A1 - Bernlöhr, K. A1 - Birsin, E. A1 - Blackwell, R. A1 - Bottcher, Markus A1 - Boisson, Catherine A1 - Bolmont, J. A1 - Bordas, Pol A1 - Bregeon, Johan A1 - Brun, Francois A1 - Brun, Pierre A1 - Bryan, Mark A1 - Bulik, Tomasz A1 - Capasso, M. A1 - Carr, John A1 - Casanova, Sabrina A1 - Chakraborty, N. A1 - Chalme-Calvet, R. A1 - Chaves, Ryan C. G. A1 - Chen, Andrew A1 - Chevalier, J. A1 - Chretien, M. A1 - Colafrancesco, Sergio A1 - Cologna, Gabriele A1 - Condon, B. A1 - Conrad, Jan A1 - Couturier, C. A1 - Cui, Y. A1 - Davids, I. D. A1 - Degrange, B. A1 - Deil, Christoph A1 - deWilt, P. A1 - Djannati-Atai, Arache A1 - Domainko, Wilfried A1 - Donath, Axel A1 - Dubus, Guillaume A1 - Dutson, Kate A1 - Dyks, J. A1 - Dyrda, M. A1 - Edwards, T. A1 - Egberts, Kathrin A1 - Eger, P. A1 - Ernenwein, J. -P. A1 - Eschbach, S. A1 - Farnier, C. A1 - Fegan, Stuart A1 - Fernandes, M. V. A1 - Fiasson, A. A1 - Fontaine, G. A1 - Foerster, A. A1 - Funk, S. A1 - Füßling, Matthias A1 - Gabici, Stefano A1 - Gajdus, M. A1 - Gallant, Y. A. A1 - Garrigoux, T. A1 - Giavitto, Gianluca A1 - Giebels, B. A1 - Glicenstein, J. F. A1 - Gottschall, Daniel A1 - Goyal, A. A1 - Grondin, M. -H. A1 - Grudzinska, M. A1 - Hadasch, Daniela A1 - Hahn, J. A1 - Hawkes, J. A1 - Heinzelmann, G. A1 - Henri, Gilles A1 - Hermann, G. A1 - Hervet, Olivier A1 - Hillert, A. A1 - Hinton, James Anthony A1 - Hofmann, Werner A1 - Hoischen, Clemens A1 - Holler, M. A1 - Horns, D. A1 - Ivascenko, Alex A1 - Jacholkowska, A. A1 - Jamrozy, Marek A1 - Janiak, M. A1 - Jankowsky, D. A1 - Jankowsky, Felix A1 - Jingo, M. A1 - Jogler, Tobias A1 - Jouvin, Lea A1 - Jung-Richardt, Ira A1 - Kastendieck, M. A. A1 - Katarzynski, Krzysztof A1 - Katz, Uli A1 - Kerszberg, D. A1 - Khelifi, B. A1 - Kieffer, M. A1 - King, J. A1 - Klepser, S. A1 - Klochkov, Dmitry A1 - Kluzniak, W. A1 - Kolitzus, D. A1 - Komin, Nu. A1 - Kosack, K. A1 - Krakau, S. A1 - Kraus, Michael A1 - Krayzel, F. A1 - Kruger, P. P. A1 - Laffon, H. A1 - Lamanna, G. A1 - Lau, Jeanie A1 - Lees, J. -P. A1 - Lefaucheur, J. A1 - Lefranc, V. A1 - Lemiere, A. A1 - Lemoine-Goumard, M. A1 - Lenain, J. -P. A1 - Leser, Eva A1 - Lohse, Thomas A1 - Lorentz, M. A1 - Lui, R. A1 - Lypova, Iryna A1 - Marandon, Vincent A1 - Marcowith, Alexandre A1 - Mariaud, C. A1 - Marx, R. A1 - Maurin, G. A1 - Maxted, N. A1 - Mayer, Michael A1 - Meintjes, Petrus Johannes A1 - Menzler, U. A1 - Meyer, Manuel A1 - Mitchell, A. M. W. A1 - Moderski, R. A1 - Mohamed, M. A1 - Mora, K. A1 - Moulin, E. A1 - Murach, T. A1 - de Naurois, Mathieu A1 - Niederwanger, F. A1 - Niemiec, J. A1 - Oakes, L. A1 - Odaka, Hirokazu A1 - Ohm, Stefan A1 - Oettl, S. A1 - Ostrowski, M. A1 - Oya, I. A1 - Padovani, Marco A1 - Panter, M. A1 - Parsons, R. D. A1 - Arribas, M. Paz A1 - Pekeur, N. W. A1 - Pelletier, G. A1 - Petrucci, P. -O. A1 - Peyaud, B. A1 - Pita, S. A1 - Poon, Helen A1 - Prokhorov, Dmitry A1 - Prokoph, Heike A1 - Puehlhofer, Gerd A1 - Punch, Michael A1 - Quirrenbach, Andreas A1 - Raab, S. A1 - Reimer, Anita A1 - Reimer, Olaf A1 - Renaud, M. A1 - de los Reyes, R. A1 - Rieger, Frank A1 - Romoli, Carlo A1 - Rosier-Lees, S. A1 - Rowell, G. A1 - Rudak, B. A1 - Rulten, C. B. A1 - Sahakian, V. A1 - Salek, David A1 - Sanchez, David A. A1 - Santangelo, Andrea A1 - Sasaki, Manami A1 - Schlickeiser, Reinhard A1 - Schussler, F. A1 - Schulz, Andreas A1 - Schwanke, U. A1 - Schwemmer, S. A1 - Seyffert, A. S. A1 - Shafi, N. A1 - Simoni, R. A1 - Sol, H. A1 - Spanier, Felix A1 - Spengler, G. A1 - Spiess, F. A1 - Stawarz, Lukasz A1 - Steenkamp, R. A1 - Stegmann, Christian A1 - Stinzing, F. A1 - Stycz, K. A1 - Sushch, Iurii A1 - Tavernet, J. -P. A1 - Tavernier, T. A1 - Taylor, A. M. A1 - Terrier, R. A1 - Tluczykont, Martin A1 - Trichard, C. A1 - Tuffs, R. A1 - van der Walt, Johan A1 - van Eldik, Christopher A1 - van Soelen, Brian A1 - Vasileiadis, Georges A1 - Veh, J. A1 - Venter, C. A1 - Viana, A. A1 - Vincent, P. A1 - Vink, Jacco A1 - Voisin, F. A1 - Voelk, Heinrich J. A1 - Vuillaume, Thomas A1 - Wadiasingh, Z. A1 - Wagner, Stefan J. A1 - Wagner, P. A1 - Wagner, R. M. A1 - White, R. A1 - Wierzcholska, Alicja A1 - Willmann, P. A1 - Woernlein, A. A1 - Wouters, Denis A1 - Yang, R. A1 - Zabalza, Victor A1 - Zaborov, D. A1 - Zacharias, M. A1 - Zdziarski, A. A. A1 - Zech, Andreas A1 - Zefi, F. A1 - Ziegler, A. A1 - Zywucka, Natalia T1 - Search for Dark Matter Annihilations towards the Inner Galactic Halo from 10 Years of Observations with HESS JF - Physical review letters N2 - The inner region of the Milky Way halo harbors a large amount of dark matter (DM). Given its proximity, it is one of the most promising targets to look for DM. We report on a search for the annihilations of DM particles using gamma-ray observations towards the inner 300 pc of the Milky Way, with the H.E.S.S. array of ground-based Cherenkov telescopes. The analysis is based on a 2D maximum likelihood method using Galactic Center (GC) data accumulated by H.E.S.S. over the last 10 years (2004-2014), and does not show any significant gamma-ray signal above background. Assuming Einasto and Navarro-Frenk-White DM density profiles at the GC, we derive upper limits on the annihilation cross section . These constraints are the strongest obtained so far in the TeV DM mass range and improve upon previous limits by a factor 5. For the Einasto profile, the constraints reach values of 6 x 10(-26) cm(3) s(-1) in the W+W- channel for a DM particle mass of 1.5 TeV, and 2 x 10(-26) cm(3) s(-1) in the tau(+)tau(-) channel for a 1 TeV mass. For the first time, ground-based gamma-ray observations have reached sufficient sensitivity to probe values expected from the thermal relic density for TeV DM particles. Y1 - 2016 U6 - https://doi.org/10.1103/PhysRevLett.117.111301 SN - 0031-9007 SN - 1079-7114 VL - 117 PB - American Physical Society CY - College Park ER - TY - GEN A1 - Abramowski, Attila A1 - Aharonian, Felix A. A1 - Benkhali, Faical Ait A1 - Akhperjanian, A. G. A1 - Angüner, Ekrem Oǧuzhan A1 - Backes, Michael A1 - Balenderan, Shangkari A1 - Balzer, Arnim A1 - Barnacka, Anna A1 - Becherini, Yvonne A1 - Tjus, Julia Becker A1 - Berge, David A1 - Bernhard, Sabrina A1 - Bernlöhr, Konrad A1 - Birsin, E. A1 - Biteau, Jonathan A1 - Böttcher, Markus A1 - Boisson, Catherine A1 - Bolmont, J. A1 - Bordas, Pol A1 - Bregeon, Johan A1 - Brun, Francois A1 - Brun, Pierre A1 - Bryan, Mark A1 - Bulik, Tomasz A1 - Carrigan, Svenja A1 - Casanova, Sabrina A1 - Chadwick, Paula M. A1 - Chakraborty, Nachiketa A1 - Chalme-Calvet, R. A1 - Chaves, Ryan C. G. A1 - Chretien, M. A1 - Colafrancesco, Sergio A1 - Cologna, Gabriele A1 - Conrad, Jan A1 - Couturier, Claire A1 - Cui, Yudong A1 - Davids, Isak Delberth A1 - Degrange, Bernhard A1 - Deil, Christoph A1 - deWilt, P. A1 - Djannati-Ataï, A. A1 - Domainko, Wilfried A1 - Donath, Axel A1 - Dubus, G. A1 - Dutson, K. A1 - Dyks, J. A1 - Dyrda, M. A1 - Edwards, Tanya A1 - Egberts, Kathrin A1 - Eger, Peter A1 - Espigat, P. A1 - Farnier, C. A1 - Fegan, Stephen A1 - Feinstein, Fabrice A1 - Fernandes, Milton Virgilio A1 - Fernandez, Diane A1 - Fiasson, A. A1 - Fontaine, Gerard A1 - Förster, Andreas A1 - Fuessling, M. A1 - Gabici, S. A1 - Gajdus, M. A1 - Gallant, Yves A. A1 - Garrigoux, Tania A1 - Giavitto, G. A1 - Giebels, Berrie A1 - Glicenstein, Jean-Francois A1 - Gottschall, Daniel A1 - Grondin, M. -H. A1 - Grudzinska, M. A1 - Hadasch, Daniela A1 - Haeffner, S. A1 - Hahn, Joachim A1 - Harris, Jonathan A1 - Heinzelmann, Götz A1 - Henri, G. A1 - Hermann, German A1 - Hervet, O. A1 - Hillert, Andreas A1 - Hinton, James Anthony A1 - Hofmann, Werner A1 - Hofverberg, Petter A1 - Holler, Markus A1 - Horns, Dieter A1 - Ivascenko, Alex A1 - Jacholkowska, A. A1 - Jahn, C. A1 - Jamrozy, Marek A1 - Janiak, M. A1 - Jankowsky, F. A1 - Jung-Richardt, I. A1 - Kastendieck, Max Anton A1 - Katarzynski, K. A1 - Katz, U. A1 - Kaufmann, S. A1 - Khelifi, B. A1 - Kieffer, Michel A1 - Klepser, S. A1 - Klochkov, Dmitry A1 - Kluzniak, W. A1 - Kolitzus, David A1 - Komin, Nu A1 - Kosack, Karl A1 - Krakau, Steffen A1 - Krayzel, F. A1 - Krueger, Pat P. A1 - Laffon, H. A1 - Lamanna, G. A1 - Lefaucheur, J. A1 - Lefranc, Valentin A1 - Lemiere, A. A1 - Lemoine-Goumard, M. A1 - Lenain, J. -P. A1 - Lohse, Thomas A1 - Lopatin, A. A1 - Lu, Chia-Chun A1 - Marandon, Vincent A1 - Marcowith, Alexandre A1 - Marx, Ramin A1 - Maurin, G. A1 - Maxted, Nigel A1 - Mayer, Michael A1 - McComb, T. J. Lowry A1 - Mehault, J. A1 - Meintjes, P. J. A1 - Menzler, Ulf A1 - Meyer, M. A1 - Mitchell, Alison M. W. A1 - Moderski, R. A1 - Mohamed, M. A1 - Mora, K. A1 - Moulin, Emmanuel A1 - Murach, Thomas A1 - de Naurois, Mathieu A1 - Niemiec, J. A1 - Nolan, Sam J. A1 - Oakes, Louise A1 - Odaka, Hirokazu A1 - Ohm, S. A1 - Optiz, Björn A1 - Ostrowski, Michal A1 - Oya, I. A1 - Panter, Michael A1 - Parsons, R. Daniel A1 - Arribas, M. Paz A1 - Pekeur, Nikki W. A1 - Pelletier, G. A1 - Petrucci, P. -O. A1 - Peyaud, B. A1 - Pita, S. A1 - Poon, Helen A1 - Pühlhofer, Gerd A1 - Punch, M. A1 - Quirrenbach, A. A1 - Raab, S. A1 - Reichardt, I. A1 - Reimer, Anita A1 - Reimer, Olaf A1 - Renaud, Metz A1 - de los Reyes, Raquel A1 - Rieger, Frank A1 - Romoli, C. A1 - Rosier-Lees, S. A1 - Rowell, G. A1 - Rudak, B. A1 - Rulten, C. B. A1 - Sahakian, Vardan A1 - Salek, D. A1 - Sanchez, David M. A1 - Santangelo, Andrea A1 - Schlickeiser, Reinhard A1 - Schuessler, F. A1 - Schulz, A. A1 - Schwanke, Ullrich A1 - Schwarzburg, S. A1 - Schwemmer, S. A1 - Sol, H. A1 - Spanier, Felix A1 - Spengler, G. A1 - Spies, Franziska A1 - Stawarz, Lukasz A1 - Steenkamp, Riaan A1 - Stegmann, Christian A1 - Stinzing, F. A1 - Stycz, K. A1 - Sushch, Iurii A1 - Tavernet, J. -P. A1 - Tavernier, T. A1 - Taylor, A. M. A1 - Terrier, R. A1 - Tluczykont, Martin A1 - Trichard, C. A1 - Valerius, K. A1 - van Eldik, C. A1 - van Soelen, B. A1 - Vasileiadis, Georges A1 - Veh, J. A1 - Venter, Christo A1 - Viana, Aion A1 - Vincent, P. A1 - Vink, Jacco A1 - Völk, Heinrich J. A1 - Volpe, Francesca A1 - Vorster, Martine A1 - Vuillaume, T. A1 - Wagner, S. J. A1 - Wagner, P. A1 - Wagner, R. M. A1 - Ward, Martin A1 - Weidinger, Matthias A1 - Weitzel, Quirin A1 - White, R. A1 - Wierzcholska, A. A1 - Willmann, P. A1 - Woernlein, A. A1 - Wouters, D. A1 - Yang, Ruizhi A1 - Zabalza, Victor A1 - Zaborov, Dmitry A1 - Zacharias, M. A1 - Zdziarski, A. A. A1 - Zech, Alraune A1 - Zechlin, Hannes -S. T1 - H.E.S.S. detection of TeV emission from the interaction region between the supernova remnant G349.7+0.2 and a molecular cloud (vol 574, A100, 2015) T2 - Astronomy and astrophysics : an international weekly journal KW - gamma rays: general KW - ISM: supernova remnants KW - ISM: clouds KW - errata, addenda Y1 - 2015 U6 - https://doi.org/10.1051/0004-6361/201425070e SN - 1432-0746 VL - 580 PB - EDP Sciences CY - Les Ulis ER - TY - JOUR A1 - Mondal, Suvendu Sekhar A1 - Dey, Subarna A1 - Attallah, Ahmed G. A1 - Krause-Rehberg, Reinhard A1 - Janiak, Christoph A1 - Holdt, Hans-Jürgen T1 - Insights into the pores of microwave-assisted metal-imidazolate frameworks showing enhanced gas sorption JF - Dalton transactions : a journal of inorganic chemistry, including bioinorganic, organometallic, and solid-state chemistry N2 - Microwave heating (MW)-assisted synthesis has been widely applied as an alternative method for the chemical synthesis of organic and inorganic materials. In this work, we report MW-assisted synthesis of three isostructural 3D frameworks with a flexible linker arm of the chelating linker 2-substituted imidazolate- 4-amide-5-imidate, named IFP-7-MW (M = Zn, R = OMe), IFP-8-MW (M = Co; R = OMe) and IFP-10-MW (M = Co; R = OEt) (IFP = Imidazolate Framework Potsdam). These chelating ligands were generated in situ by partial hydrolysis of 2-substituted 4,5-dicyanoimidazoles under MW-and also conventional electrical heating (CE)-assisted conditions in DMF. The structure of these materials was determined by IR spectroscopy and powder X-ray diffraction (PXRD) and the identity of the materials synthesized under CE-conditions was established. Materials obtained from MW-heating show many fold enhancement of CO2 and H-2 uptake capacities, compared to the analogous CE-heating method based materials. To understand the inner pore-sizes of IFP structures and variations of gas sorptions, we performed positron annihilation lifetime spectroscopy (PALS), which shows that MW-assisted materials have smaller pore sizes than materials synthesized under CE-conditions. The "kinetically controlled" MW-synthesized material has an inherent ability to trap extra linkers, thereby reducing the pore sizes of CE-materials to ultra/micropores. These ultramicropores are responsible for high gas sorption. Y1 - 2017 U6 - https://doi.org/10.1039/c7dt00350a SN - 1477-9226 SN - 1477-9234 VL - 46 SP - 4824 EP - 4833 PB - Royal Society of Chemistry CY - Cambridge ER - TY - JOUR A1 - Alrefai, Anas A1 - Mondal, Suvendu Sekhar A1 - Wruck, Alexander A1 - Kelling, Alexandra A1 - Schilde, Uwe A1 - Brandt, Philipp A1 - Janiak, Christoph A1 - Schoenfeld, Sophie A1 - Weber, Birgit A1 - Rybakowski, Lawrence A1 - Herrman, Carmen A1 - Brennenstuhl, Katlen A1 - Eidner, Sascha A1 - Kumke, Michael Uwe A1 - Behrens, Karsten A1 - Günter, Christina A1 - Müller, Holger A1 - Holdt, Hans-Jürgen T1 - Hydrogen-bonded supramolecular metal-imidazolate frameworks: gas sorption, magnetic and UV/Vis spectroscopic properties JF - Journal of Inclusion Phenomena and Macrocyclic Chemistry N2 - By varying reaction parameters for the syntheses of the hydrogen-bonded metal-imidazolate frameworks (HIF) HIF-1 and HIF-2 (featuring 14 Zn and 14 Co atoms, respectively) to increase their yields and crystallinity, we found that HIF-1 is generated in two different frameworks, named as HIF-1a and HIF-1b. HIF-1b is isostructural to HIF-2. We determined the gas sorption and magnetic properties of HIF-2. In comparison to HIF-1a (Brunauer-Emmett-Teller (BET) surface area of 471m(2) g(-1)), HIF-2 possesses overall very low gas sorption uptake capacities [BET(CO2) surface area=85m(2) g(-1)]. Variable temperature magnetic susceptibility measurement of HIF-2 showed antiferromagnetic exchange interactions between the cobalt(II) high-spin centres at lower temperature. Theoretical analysis by density functional theory confirmed this finding. The UV/Vis-reflection spectra of HIF-1 (mixture of HIF-1a and b), HIF-2 and HIF-3 (with 14 Cd atoms) were measured and showed a characteristic absorption band centered at 340nm, which was indicative for differences in the imidazolate framework. KW - Gas-sorption KW - Ligand design KW - Magnetic properties KW - Supramolecular chemistry KW - Solvothermal synthesis Y1 - 2019 U6 - https://doi.org/10.1007/s10847-019-00926-6 SN - 1388-3127 SN - 1573-1111 VL - 94 IS - 3-4 SP - 155 EP - 165 PB - Springer CY - Dordrecht ER - TY - GEN A1 - Mondal, Suvendu Sekhar A1 - Marquardt, Dorothea A1 - Janiak, Christoph A1 - Holdt, Hans-Jürgen T1 - Use of a 4,5-dicyanoimidazolate anion based ionic liquid for the synthesis of iron and silver nanoparticles N2 - Sixteen new ionic liquids (ILs) with tetraethylammonium, 1-butyl-3-methylimidazolium, 3-methyl-1-octylimidazolium and tetrabutylphosphonium cations paired with 2-substituted 4,5-dicyanoimidazolate anions (substituent at C2 = methyl, trifluoromethyl, pentafluoroethyl, N,N′-dimethyl amino and nitro) have been synthesized and characterized by using differential scanning calorimetry (DSC), thermogravimetric analysis (TGA). The effects of cation and anion type and structure of the resulting ILs, including several room temperature ionic liquids (RTILs), are reflected in the crystallization, melting points and thermal decomposition of the ILs. ILs exhibited large liquid and crystallization ranges and formed glasses on cooling with glass transition temperatures in the range of −22 to −71 °C. We selected one of the newly designed ILs due to its bigger size, compared to the common conventional IL anion and high electron-withdrawing nitrile group leads to an overall stabilization anion that may stabilize the metal nanoparticles. Stable and better separated iron and silver nanoparticles are obtained by the decomposition of corresponding Fe2(CO)9 and AgPF6, respectively, under N2-atmosphere in newly designed nitrile functionalized 4,5-dicyanoimidazolate anion based IL. Very small and uniform size for Fe-nanoparticles of about 1.8 ± 0.6 nm were achieved without any additional stabilizers or capping molecules. Comparatively bigger size of Ag-nanoparticles was obtained through the reduction of AgPF6 by hydrogen gas. Additionally, the AgPF6 precursor was decomposed under microwave irradiation (MWI), fabricating nut-in-shell-like, that is, core-separated-from-shell Ag-nano-structures. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 220 Y1 - 2016 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-89696 SP - 5476 EP - 5483 ER - TY - GEN A1 - Mondal, Suvendu Sekhar A1 - Dey, Subarna A1 - Baburin, Igor A. A1 - Kelling, Alexandra A1 - Schilde, Uwe A1 - Seifert, Gotthard A1 - Janiak, Christoph A1 - Holdt, Hans-Jürgen T1 - Syntheses of two imidazolate-4-amide-5-imidate linker-based hexagonal metal–organic frameworks with flexible ethoxy substituent N2 - A rare example of in situ linker generation with the formation of soft porous Zn- and Co-MOFs (IFP-9 and -10, respectively) is reported. The flexible ethoxy groups of IFP-9 and -10 protrude into the 1D hexagonal channels. The gas-sorption behavior of both materials for H2, CO2 and CH4 showed wide hysteretic isotherms, typical for MOFs having a flexible substituent which can give rise to a gate effect. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 234 KW - adsorption KW - behavior KW - carbon-dioxide KW - crystals KW - gases KW - ligand KW - pressure KW - selectivity KW - temperature KW - zinc Y1 - 2013 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-94360 SP - 9394 EP - 9399 ER - TY - GEN A1 - Mondal, Suvendu Sekhar A1 - Bhunia, Asamanjoy A1 - Demeshko, Serhiy A1 - Kelling, Alexandra A1 - Schilde, Uwe A1 - Janiak, Christoph A1 - Holdt, Hans-Jürgen T1 - Synthesis of a Co(II)–imidazolate framework from an anionic linker precursor BT - gas-sorption and magnetic properties N2 - A Co(II)–imidazolate-4-amide-5-imidate based MOF, IFP-5, is synthesized by using an imidazolate anion-based novel ionic liquid as a linker precursor under solvothermal conditions. IFP-5 shows significant amounts of gas (N2, CO2, CH4 and H2) uptake capacities. IFP-5 exhibits an independent high spin Co(II) centre and antiferromagnetic coupling. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 235 KW - building-blocks KW - carbon-dioxide capture KW - exchange KW - ionic liquids KW - ionothermal synthesis KW - ligand KW - metal-organic frameworks KW - solvent KW - surface KW - zeolitic imidazolate frameworks Y1 - 2013 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-94424 SP - 39 EP - 42 ER - TY - GEN A1 - Mondal, Suvendu Sekhar A1 - Bhunia, Asamanjoy A1 - Kelling, Alexandra A1 - Schilde, Uwe A1 - Janiak, Christoph A1 - Holdt, Hans-Jürgen T1 - A supramolecular Co(II)₁₄-metal–organic cube in a hydrogen-bonded network and a Co(II)–organic framework with a flexible methoxy substituent N2 - The reaction of 4,5-dicyano-2-methoxyimidazole (L1) with Co(NO3)2·6H2O under solvothermal conditions in DMF, a MOF, IFP-8 and a hydrogen-bonded network consisting of tetradecanuclear Co(II)14-metal organic cube (1) are achieved. 1 shows the bcu net with 14 cobalt atoms. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - paper 169 KW - zinc Y1 - 2014 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-74098 IS - 169 SP - 5441 EP - 5443 ER - TY - GEN A1 - Mondal, Suvendu Sekhar A1 - Bhunia, Asamanjoy A1 - Baburin, Igor A. A1 - Jäger, Christian A1 - Kelling, Alexandra A1 - Schilde, Uwe A1 - Seifert, Gotthard A1 - Janiak, Christoph A1 - Holdt, Hans-Jürgen T1 - Gate effects in a hexagonal zinc-imidazolate-4-amide-5-imidate framework with flexible methoxy substituents and CO2 selectivity N2 - A new imidazolate-4-amide-5-imidate based MOF, IFP-7, is generated, having flexible methoxy groups, which act as molecular gates for guest molecules. This allows highly selective CO2 sorption over N2 and CH4 gases. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 233 KW - adsorption KW - capacity KW - carbon-dioxide capture KW - coordination polymer KW - flexibility KW - hydrogen storage KW - ligand KW - metal-organic frameworks KW - mixed-matrix membranes KW - separation Y1 - 2013 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-94341 SP - 7599 EP - 7601 ER - TY - JOUR A1 - Mondal, Suvendu Sekhar A1 - Marquardt, Dorothea A1 - Janiak, Christoph A1 - Holdt, Hans-Jürgen T1 - Use of a 4,5-dicyanoimidazolate anion based ionic liquid for the synthesis of iron and silver nanoparticles JF - Dalton transactions : an international journal of inorganic chemistry N2 - Sixteen new ionic liquids (ILs) with tetraethylammonium, 1-butyl-3-methylimidazolium, 3-methyl-1-octylimidazolium and tetrabutylphosphonium cations paired with 2-substituted 4,5-dicyanoimidazolate anions (substituent at C2 = methyl, trifluoromethyl, pentafluoroethyl, N,N′-dimethyl amino and nitro) have been synthesized and characterized by using differential scanning calorimetry (DSC), thermogravimetric analysis (TGA). The effects of cation and anion type and structure of the resulting ILs, including several room temperature ionic liquids (RTILs), are reflected in the crystallization, melting points and thermal decomposition of the ILs. ILs exhibited large liquid and crystallization ranges and formed glasses on cooling with glass transition temperatures in the range of −22 to −71 °C. We selected one of the newly designed ILs due to its bigger size, compared to the common conventional IL anion and high electron-withdrawing nitrile group leads to an overall stabilization anion that may stabilize the metal nanoparticles. Stable and better separated iron and silver nanoparticles are obtained by the decomposition of corresponding Fe2(CO)9 and AgPF6, respectively, under N2-atmosphere in newly designed nitrile functionalized 4,5-dicyanoimidazolate anion based IL. Very small and uniform size for Fe-nanoparticles of about 1.8 ± 0.6 nm were achieved without any additional stabilizers or capping molecules. Comparatively bigger size of Ag-nanoparticles was obtained through the reduction of AgPF6 by hydrogen gas. Additionally, the AgPF6 precursor was decomposed under microwave irradiation (MWI), fabricating nut-in-shell-like, that is, core-separated-from-shell Ag-nano-structures. Y1 - 2016 U6 - https://doi.org/10.1039/C6DT00225K SN - 1477-9226 IS - 45 SP - 5476 EP - 5483 PB - Royal Society of Chemistry CY - Cambridge ER - TY - JOUR A1 - Mondal, Suvendu Sekhar A1 - Bhunia, Asamanjoy A1 - Kelling, Alexandra A1 - Schilde, Uwe A1 - Janiak, Christoph A1 - Holdt, Hans-Jürgen T1 - A supramolecular Co(II)₁₄-metal–organic cube in a hydrogen-bonded network and a Co(II)–organic framework with a flexible methoxy substituent JF - Chemical communications : ChemComm N2 - The reaction of 4,5-dicyano-2-methoxyimidazole (L1) with Co(NO3)2·6H2O under solvothermal conditions in DMF, a MOF, IFP-8 and a hydrogen-bonded network consisting of tetradecanuclear Co(II)14-metal organic cube (1) are achieved. 1 shows the bcu net with 14 cobalt atoms. KW - zinc Y1 - 2014 U6 - https://doi.org/10.1039/c3cc49698h SN - 2046-2069 VL - 2014 IS - 41 SP - 5441 EP - 5443 PB - Royal Society of Chemistry ER - TY - JOUR A1 - Mondal, Suvendu Sekhar A1 - Dey, Subarna A1 - Baburin, Igor A. A1 - Kelling, Alexandra A1 - Schilde, Uwe A1 - Seifert, Gotthard A1 - Janiak, Christoph A1 - Holdt, Hans-Jürgen T1 - Syntheses of two imidazolate-4-amide-5-imidate linker-based hexagonal metal-organic frameworks with flexible ethoxy substituent JF - CrystEngComm N2 - A rare example of in situ linker generation with the formation of soft porous Zn- and Co-MOFs (IFP-9 and -10, respectively) is reported. The flexible ethoxy groups of IFP-9 and -10 protrude into the 1D hexagonal channels. The gas-sorption behavior of both materials for H-2, CO2 and CH4 showed wide hysteretic isotherms, typical for MOFs having a flexible substituent which can give rise to a gate effect. Y1 - 2013 U6 - https://doi.org/10.1039/c3ce41632a SN - 1466-8033 VL - 15 IS - 45 SP - 9394 EP - 9399 PB - Royal Society of Chemistry CY - Cambridge ER - TY - JOUR A1 - Mondal, Suvendu Sekhar A1 - Bhunia, Asamanjoy A1 - Baburin, Igor A. A1 - Jäger, Christian A1 - Kelling, Alexandra A1 - Schilde, Uwe A1 - Seifert, Gotthard A1 - Janiak, Christoph A1 - Holdt, Hans-Jürgen T1 - Gate effects in a hexagonal zinc-imidazolate-4-amide-5-imidate framework with flexible methoxy substituents and CO2 selectivity JF - Chemical communications N2 - A new imidazolate-4-amide-5-imidate based MOF, IFP-7, is generated, having flexible methoxy groups, which act as molecular gates for guest molecules. This allows highly selective CO2 sorption over N-2 and CH4 gases. Y1 - 2013 U6 - https://doi.org/10.1039/c3cc42156b SN - 1359-7345 VL - 49 IS - 69 SP - 7599 EP - 7601 PB - Royal Society of Chemistry CY - Cambridge ER - TY - JOUR A1 - Mondal, Suvendu Sekhar A1 - Dey, Subarna A1 - Baburin, Igor A. A1 - Kelling, Alexandra A1 - Schilde, Uwe A1 - Janiak, Christoph A1 - Holdt, Hans-Jürgen T1 - Syntheses of two imidazolate-4-amide-5-imidate linker based hexagonal metal-organic frameworks with flexible ethoxy substituent N2 - A rare example of in situ linker generation with the formation of soft porous Zn- and Co-MOFs (IFP-9 and -10, respectively) is reported. The flexible ethoxy groups of IFP-9 and -10 protrude into the 1D hexagonal channels. The gas- sorption behavior of both materials for H2, CO2 and CH4 showed wide hysteretic isotherms, typical for MOFs having a flexible substituent which can give rise to a gate effect. Y1 - 2008 UR - http://pubs.rsc.org/en/Content/ArticleLanding/2013/CE/c3ce41632a U6 - https://doi.org/10.1039/C3CE41632A ER - TY - JOUR A1 - Mondal, Suvendu Sekhar A1 - Bhunia, Asamanjoy A1 - Demeshok, Serhiy A1 - Kelling, Alexandra A1 - Schilde, Uwe A1 - Janiak, Christoph A1 - Holdt, Hans-Jürgen T1 - Synthesis of a Co(II)-imidazolate framework from an anionic linker precursor: gas-sorption ans magnetic proberties N2 - A Co(II)-imidazolate-4-amide-5-imidate based MOF, IFP-5, is synthesized by using an imidazolate anion-based novel ionic liquid as a linker precursor under solvothermal conditions. IFP-5 shows significant amounts of gas (N2, CO2, CH4 and H2) uptake capacities. IFP-5 exhibits an independent high spin Co(II) centre and antiferromagnetic coupling. Y1 - 2008 UR - http://pubs.rsc.org/en/content/articlelanding/2013/ce/c3ce42040j ER - TY - JOUR A1 - Mondal, Suvendu Sekhar A1 - Bhunia, Asamanjoy A1 - Baburin, Igor A. A1 - Jäger, Christian A1 - Kelling, Alexandra A1 - Schilde, Uwe A1 - Seiert, Gotthard A1 - Janiak, Christoph A1 - Holdt, Hans-Jürgen T1 - Gate effects in a hexagonal zinc-imidazolate-4-amide-5-imidate framework with flexible methoxy substituents and CO2 selectivity N2 - A new imidazolate-4-amide-5-imidate based MOF, IFP-7, is generated, having flexible methoxy groups, which act as molecular gates for guest molecules. This allows highly selective CO2 sorption over N2 and CH4 gases. Y1 - 2008 UR - http://pubs.rsc.org/en/content/articlepdf/2013/cc/c3cc42156b U6 - https://doi.org/10.1039/C3CC42156B ER - TY - JOUR A1 - Mondal, Suvendu Sekhar A1 - Bhunia, Asamanjoy A1 - Attallah, Ahmed G. A1 - Matthes, Philipp R. A1 - Kelling, Alexandra A1 - Schilde, Uwe A1 - Müller-Buschbaum, Klaus A1 - Krause-Rehberg, Reinhard A1 - Janiak, Christoph A1 - Holdt, Hans-Jürgen T1 - Study of the Discrepancies between Crystallographic Porosity and Guest Access into Cadmium-Imidazolate Frameworks and Tunable Luminescence Properties by Incorporation of Lanthanides JF - Chemistry - a European journal N2 - An extended member of the isoreticular family of metal-imidazolate framework structures, IFP-6 (IFP=imidazolate framework Potsdam), based on cadmium metal and an in situ functionalized 2-methylimidazolate-4-amide-5-imidate linker is reported. A porous 3D framework with 1D hexagonal channels with accessible pore windows of 0.52nm has been synthesized by using an ionic liquid (IL) linker precursor. IFP-6 shows significant gas uptake capacity only for CO2 and CH4 at elevated pressure, whereas it does not adsorb N-2, H-2, and CH4 under atmospheric conditions. IFP-6 is assumed to deteriorate at the outside of the material during the activation process. This closing of the metal-organic framework (MOF) pores is proven by positron annihilation lifetime spectroscopy (PALS), which revealed inherent crystal defects. PALS results support the conservation of the inner pores of IFP-6. IFP-6 has also been successfully loaded with luminescent trivalent lanthanide ions (Ln(III)=Tb, Eu, and Sm) in a bottom-up one-pot reaction through the in situ generation of the linker ligand and in situ incorporation of photoluminescent Ln ions into the constituting network. The results of photoluminescence investigations and powder XRD provide evidence that the Ln ions are not doped as connectivity centers into the frameworks, but are instead located within the pores of the MOFs. Under UV light irradiation, Tb@IFP-6 and Eu@IFP-6 ((exc)=365nm) exhibit observable emission changes to a greenish and reddish color, respectively, as a result of strong Ln 4f emissions. KW - adsorption KW - cadmium KW - ionic liquids KW - luminescence KW - metal-organic frameworks Y1 - 2016 U6 - https://doi.org/10.1002/chem.201504757 SN - 0947-6539 SN - 1521-3765 VL - 22 SP - 6905 EP - 6913 PB - Wiley-VCH CY - Weinheim ER - TY - JOUR A1 - Mondal, Suvendu Sekhar A1 - Bhunia, Asamanjoy A1 - Kelling, Alexandra A1 - Schilde, Uwe A1 - Janiak, Christoph A1 - Holdt, Hans-Jürgen T1 - Giant Zn-14 molecular building block in hydrogen-bonded network with permanent porosity for gas uptake JF - Journal of the American Chemical Society N2 - In situ imidazolate-4,5-diamide-2-olate linker generation leads to the formation of a [Zn-14(L2)(12)(O)-(OH)(2)(H2O)(4)] molecular building block (MBB) with a Zn-6 octahedron inscribed in a Zn-8 cube. The MBBs connect by amide-amide hydrogen bonds to a 3D robust supramolecular network which can be activated for N-2, CO2, CH4, and H-2 gas sorption. Y1 - 2014 U6 - https://doi.org/10.1021/ja410595q SN - 0002-7863 VL - 136 IS - 1 SP - 44 EP - 47 PB - American Chemical Society CY - Washington ER - TY - JOUR A1 - Mondal, Suvendu Sekhar A1 - Bhunia, Asamanjoy A1 - Kelling, Alexandra A1 - Schilde, Uwe A1 - Janiak, Christoph A1 - Holdt, Hans-Jürgen T1 - A supramolecular Co(II)(14)- metal-organic cube in a hydrogen-bonded network and a Co(II)-organic framework with a flexible methoxy substituent JF - Chemical communications N2 - The reaction of 4,5-dicyano-2-methoxyimidazole (L1) with Co(NO3)(2.) 6H(2)O under solvothermal conditions in DMF, a MOF, IFP-8 and a hydrogen-bonded network consisting of tetradecanuclear Co(II)(14)-metal organic cube (1) are achieved. 1 shows the bcu net with 14 cobalt atoms. Y1 - 2014 U6 - https://doi.org/10.1039/c3cc49698h SN - 1359-7345 SN - 1364-548X VL - 50 IS - 41 SP - 5441 EP - 5443 PB - Royal Society of Chemistry CY - Cambridge ER - TY - JOUR A1 - Mondal, Suvendu Sekhar A1 - Bhunia, Asamanjoy A1 - Demeshko, Serhiy A1 - Kelling, Alexandra A1 - Schilde, Uwe A1 - Janiak, Christoph A1 - Holdt, Hans-Jürgen T1 - Synthesis of a Co(II)-imidazolate framework from an anionic linker precursor: gas-sorption and magnetic properties JF - CrystEngComm N2 - A Co(II)-imidazolate-4-amide-5-imidate based MOF, IFP-5, is synthesized by using an imidazolate anion-based novel ionic liquid as a linker precursor under solvothermal conditions. IFP-5 shows significant amounts of gas (N-2, CO2, CH4 and H-2) uptake capacities. IFP-5 exhibits an independent high spin Co(II) centre and antiferromagnetic coupling. Y1 - 2014 U6 - https://doi.org/10.1039/c3ce42040j SN - 1466-8033 VL - 16 IS - 1 SP - 39 EP - 42 PB - Royal Society of Chemistry CY - Cambridge ER - TY - JOUR A1 - Mondal, Suvendu Sekhar A1 - Marquardt, Dorothea A1 - Janiak, Christoph A1 - Holdt, Hans-Jürgen T1 - Use of a 4,5-dicyanoimidazolate anion based ionic liquid for the synthesis of iron and silver nanoparticles JF - Dalton transactions : a journal of inorganic chemistry, including bioinorganic, organometallic, and solid-state chemistry N2 - Sixteen new ionic liquids (ILs) with tetraethylammonium, 1-butyl-3-methylimidazolium, 3-methyl-1-octylimidazolium and tetrabutylphosphonium cations paired with 2-substituted 4,5-dicyanoimidazolate anions (substituent at C2 = methyl, trifluoromethyl, pentafluoroethyl, N,N′-dimethyl amino and nitro) have been synthesized and characterized by using differential scanning calorimetry (DSC), thermogravimetric analysis (TGA). The effects of cation and anion type and structure of the resulting ILs, including several room temperature ionic liquids (RTILs), are reflected in the crystallization, melting points and thermal decomposition of the ILs. ILs exhibited large liquid and crystallization ranges and formed glasses on cooling with glass transition temperatures in the range of −22 to −71 °C. We selected one of the newly designed ILs due to its bigger size, compared to the common conventional IL anion and high electron-withdrawing nitrile group leads to an overall stabilization anion that may stabilize the metal nanoparticles. Stable and better separated iron and silver nanoparticles are obtained by the decomposition of corresponding Fe2(CO)9 and AgPF6, respectively, under N2-atmosphere in newly designed nitrile functionalized 4,5-dicyanoimidazolate anion based IL. Very small and uniform size for Fe-nanoparticles of about 1.8 ± 0.6 nm were achieved without any additional stabilizers or capping molecules. Comparatively bigger size of Ag-nanoparticles was obtained through the reduction of AgPF6 by hydrogen gas. Additionally, the AgPF6 precursor was decomposed under microwave irradiation (MWI), fabricating nut-in-shell-like, that is, core-separated-from-shell Ag-nano-structures. Y1 - 2016 U6 - https://doi.org/10.1039/c6dt00225k SN - 1477-9226 SN - 1477-9234 VL - 45 SP - 5476 EP - 5483 PB - Royal Society of Chemistry CY - Cambridge ER - TY - JOUR A1 - Mondal, Suvendu Sekhar A1 - Hovestadt, Maximilian A1 - Dey, Subarna A1 - Paula, Carolin A1 - Glomb, Sebastian A1 - Kelling, Alexandra A1 - Schilde, Uwe A1 - Janiak, Christoph A1 - Hartmann, Martin A1 - Holdt, Hans-Jürgen T1 - Synthesis of a partially fluorinated ZIF-8 analog for ethane/ethene separation JF - CrystEngComm N2 - The separation of ethane/ethene mixtures (as well as other paraffin/olefin mixtures) is one of the most important but challenging processes in the petrochemical industry. In this work, we report the synthesis of ZIF-318, isostructural to ZIF-8 but built from the mixed linkers of 2-methylimidazole (L1) and 2-trifluoromethylimidazole (L2) (ZIF-318 = [(Zn(L1)(L2)](n)). The synthesis has been optimized to proceed without ZnO-formation. Using only the L2 linker under solvothermal conditions afforded ZnO-embedded in the H-bonded and non-porous coordination polymer ZnO@[Zn-2(L2)(2)(HCOO)(OH)](n). The slight differences in the size of the substituents (-CH3 vs. -CF3) possibly in combination with different electronic inductive effects led to small but significant changes to the pore size and properties respectively, though the effective pore opening (aperture) size of ZIF-318 remained the same in comparison with ZIF-8. ZIF-318 is chemically (boiling water, methanol, benzene, and wide pH range at room temperature for 1 day), thermally (up to 310 degrees C) stable, and more hydrophobic than ZIF-8 which is proven by contact angle measurement. ZIF-318 can be activated for N-2, CO2, CH4, H-2, ethane, ethane, propane, and propene gases sorptions. Consequently, in breakthrough experiments, the ethane/ethene mixtures can be separated. Y1 - 2017 U6 - https://doi.org/10.1039/c7ce01438d SN - 1466-8033 VL - 19 SP - 5882 EP - 5891 PB - Royal Society of Chemistry CY - Cambridge ER - TY - JOUR A1 - Marquardt, Dorothea A1 - Xie, Zailai A1 - Taubert, Andreas A1 - Thomann, Ralf A1 - Janiak, Christoph T1 - Microwave synthesis and inherent stabilization of metal nanoparticles in 1-methyl-3-(3-carboxyethyl)-imidazolium tetrafluoroborate JF - Dalton transactions : a journal of inorganic chemistry, including bioinorganic, organometallic, and solid-state chemistry N2 - The synthesis of Co-NPs and Mn-NPs by microwave-induced decomposition of the metal carbonyls Co-2(CO)(8) and Mn-2(CO)(10), respectively, yields smaller and better separated particles in the functionalized IL 1-methyl-3-(3-carboxyethyl)-imidazolium tetrafluoroborate [EmimCO(2)H][BF4] (1.6 +/- 0.3 nm and 4.3 +/- 1.0 nm, respectively) than in the non-functionalized IL 1-n-butyl-3-methylimidazolium tetrafluoroborate [Bmim][BF4]. The particles are stable in the absence of capping ligands (surfactants) for more than six months although some variation in particle size could be observed by TEM. Y1 - 2011 U6 - https://doi.org/10.1039/c1dt10795j SN - 1477-9226 VL - 40 IS - 33 SP - 8290 EP - 8293 PB - Royal Society of Chemistry CY - Cambridge ER -