Search Results - "Gruber, Irina"

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  1. 1

    Three‐Component Activation/Alkynylation/Cyclocondensation (AACC) Synthesis of Enhanced Emission Solvatochromic 3‐Ethynylquinoxalines by Merkt, Franziska K., Höwedes, Simon P., Gers‐Panther, Charlotte F., Gruber, Irina, Janiak, Christoph, Müller, Thomas J. J.

    Published in Chemistry : a European journal (07-06-2018)
    “…2‐Substituted 3‐ethynylquinoxaline chromophores can be readily synthesized by a consecutive activation–alkynylation–cyclocondensation (AACC) one‐pot sequence…”
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    Journal Article
  2. 2

    5‐(Hetero)aryl‐Substituted 9‐Hydroxyphenalenones: Synthesis and Electronic Properties of Multifunctional Donor–Acceptor Conjugates by Bensch, Lisa, Gruber, Irina, Janiak, Christoph, Müller, Thomas J. J.

    Published in Chemistry : a European journal (04-08-2017)
    “…5‐(Hetero)aryl‐substituted 9‐hydroxyphenalenones (9‐HP) can be readily synthesized by Suzuki coupling of 5‐bromo 9‐HP with (hetero)aryl boronic acid…”
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    Journal Article
  3. 3

    Emission solvatochromic, solid-state and aggregation-induced emissive α-pyrones and emission-tuneable 1H-pyridines by Michael addition–cyclocondensation sequences by Breuer Natascha, Gruber, Irina, Janiak Christoph, Müller Thomas J J

    Published in Beilstein journal of organic chemistry (12-11-2019)
    “…Starting from substituted alkynones, α-pyrones and/or 1H-pyridines were generated in a Michael addition–cyclocondensation with ethyl cyanoacetate. The peculiar…”
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    Journal Article
  4. 4

    Synthesis of Nano/Microsized MIL-101Cr Through Combination of Microwave Heating and Emulsion Technology for Mixed-Matrix Membranes by Gruber, Irina, Nuhnen, Alexander, Lerch, Arne, Nießing, Sandra, Klopotowski, Maximilian, Herbst, Annika, Karg, Matthias, Janiak, Christoph

    Published in Frontiers in chemistry (19-11-2019)
    “…Nano/microsized MIL-101Cr was synthesized by microwave heating of emulsions for the use as a composite with Matrimid mixed-matrix membranes (MMM) to enhance…”
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    Journal Article
  5. 5

    Facile synthesis of nano-sized MIL-101(Cr) with the addition of acetic acid by Zhao, Tian, Yang, Ling, Feng, Peiyong, Gruber, Irina, Janiak, Christoph, Liu, Yuejun

    Published in Inorganica Chimica Acta (24-02-2018)
    “…[Display omitted] •A new method for synthesis of nano-MIL-101(Cr) with high-surface area is proposed.•The particle size of MIL-101(Cr) can be facilely…”
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  6. 6

    Urea-based flexible dicarboxylate linkers for three-dimensional metal-organic frameworks by Glomb, Sebastian, Makhloufi, Gamall, Gruber, Irina, Janiak, Christoph

    Published in Inorganica Chimica Acta (24-04-2018)
    “…[Display omitted] •First examples of 3D-MOFs with single urea-based ditopic dicarboxylate linker.•Isostructural 3D-MOFs of diamond (6,6), dia…”
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  7. 7

    Silver, Gold, Palladium, and Platinum N‑heterocyclic Carbene Complexes Containing a Selenoether-Functionalized Imidazol-2-ylidene Moiety by Klauke, Karsten, Gruber, Irina, Knedel, Tim-Oliver, Schmolke, Laura, Barthel, Juri, Breitzke, Hergen, Buntkowsky, Gerd, Janiak, Christoph

    Published in Organometallics (12-02-2018)
    “…The selenoether-functionalized imidazolium salt N-[(phenylseleno)­methylene)]-N′-methylimidazolium chloride (LH+Cl–) was transformed into the metal–carbene…”
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    Journal Article
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    Mesoxalate-Bridged Heptanuclear Copper(II) Complexes: Structure and Magnetic Properties by Gil-Hernández, Beatriz, Millan, Simon, Gruber, Irina, Janiak, Christoph, Gómez-García, Carlos J., Sanchiz, Joaquín

    Published in Magnetochemistry (22-11-2024)
    “…Two new compounds, (NH4)4[Cu7(Hmesox)6(H2O)8]∙10H2O (1) and [Ru(bpy)3]4[Cu7(Hmesox)6Cl2]Cl2∙2CH3CN∙12H2O (2), were prepared and their structures were solved by…”
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    Improvement of the Proton Conduction of Copper(II)-Mesoxalate Metal–Organic Frameworks by Strategic Selection of the Counterions by Gil-Hernández, Beatriz, Millan, Simon, Gruber, Irina, Quirós, Miguel, Marrero-López, David, Janiak, Christoph, Sanchiz, Joaquín

    Published in Inorganic chemistry (01-08-2022)
    “…Three copper­(II)/mesoxalate-based MOFs with formulas (H3O)­[Cu9(Hmesox)6(H2O)6Cl]·8H2O (1), (NH2Me2)0.4(H3O)0.6[Cu9(Hmesox)6(H2O)6Cl]·8H2O (2), and…”
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  13. 13

    Emission solvatochromic, solid-state and aggregation-induced emissive α-pyrones and emission-tuneable 1 H -pyridines by Michael addition-cyclocondensation sequences by Breuer, Natascha, Gruber, Irina, Janiak, Christoph, Müller, Thomas J J

    Published in Beilstein journal of organic chemistry (12-11-2019)
    “…Starting from substituted alkynones, α-pyrones and/or 1 -pyridines were generated in a Michael addition-cyclocondensation with ethyl cyanoacetate. The peculiar…”
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    Journal Article
  14. 14

    Inside Cover: 5‐(Hetero)aryl‐Substituted 9‐Hydroxyphenalenones: Synthesis and Electronic Properties of Multifunctional Donor–Acceptor Conjugates (Chem. Eur. J. 44/2017) by Bensch, Lisa, Gruber, Irina, Janiak, Christoph, Müller, Thomas J. J.

    Published in Chemistry : a European journal (04-08-2017)
    “…The universe of donor and acceptor building blocks is often nonluminescent. However, if linked together by our protection‐group‐free Suzuki coupling as an…”
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    Journal Article
  15. 15

    Front Cover: Three‐Component Activation/Alkynylation/Cyclocondensation (AACC) Synthesis of Enhanced Emission Solvatochromic 3‐Ethynylquinoxalines (Chem. Eur. J. 32/2018) by Merkt, Franziska K., Höwedes, Simon P., Gers‐Panther, Charlotte F., Gruber, Irina, Janiak, Christoph, Müller, Thomas J. J.

    Published in Chemistry : a European journal (07-06-2018)
    “…Fluorescent polarity sensors are rapidly and efficiently assembled from (hetero)aryl α‐ketoacids, terminal alkynes, and 1,2‐diamino arenes in a consecutive…”
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    Three‐Component Activation/Alkynylation/Cyclocondensation (AACC) Synthesis of Enhanced Emission Solvatochromic 3‐Ethynylquinoxalines by Merkt, Franziska K., Höwedes, Simon P., Gers‐Panther, Charlotte F., Gruber, Irina, Janiak, Christoph, Müller, Thomas J. J.

    Published in Chemistry : a European journal (07-06-2018)
    “…Invited for the cover of this issue is the group of Thomas J. J. Müller at the Heinrich‐Heine‐Universität Düsseldorf. The image depicts some of the fluorescent…”
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    Journal Article
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