Search Results - "Biesen, Lukas"

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  1. 1

    The complexometric behavior of selected aroyl-S,N-ketene acetals shows that they are more than AIEgens by Biesen, Lukas, Müller, Thomas J. J.

    Published in Scientific reports (31-05-2024)
    “…Using the established synthetic methods, aroyl- S , N -ketene acetals and subsequent bi- and multichromophores can be readily synthesized. Aside from…”
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    Journal Article
  2. 2

    Alkynylated and triazole-linked aroyl-S,N-ketene acetals: one-pot synthesis of solid-state emissive dyes with aggregation-induced enhanced emission characteristics by Biesen, Lukas, Hartmann, Yannic, Müller, Thomas J. J.

    Published in Scientific reports (01-09-2023)
    “…Alkynylated aroyl- S , N -ketene acetals are readily synthesized in mostly excellent yields by a Sonogashira reaction resulting in a substance library of more…”
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    Journal Article
  3. 3

    Solid‐state emissive biphenylene bridged bisaroyl‐S,N‐ketene acetals as distinct aggregation‐induced enhanced emitters and fluorometric probes by Biesen, Lukas, Müller, Thomas J. J.

    Published in Aggregate (Hoboken) (01-10-2021)
    “…Biphenylene bridged bisaroyl‐S,N‐ketene acetals can be readily synthesized by a one‐pot Masuda borylation‐Suzuki arylation sequence, thus, yielding a library…”
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    Journal Article
  4. 4

    Multicomponent and One‐pot Syntheses of Quinoxalines by Biesen, Lukas, Müller, Thomas J. J.

    Published in Advanced synthesis & catalysis (16-02-2021)
    “…Quinoxalines represent bicyclic nitrogen‐containing heterocycles with a wide array of applications. They exhibit a multitude of biological activities relevant…”
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    Journal Article
  5. 5

    Cover Feature: Solid‐State Emission and Aggregate Emission of Aroyl‐ S,N‐Ketene Acetals Are Controlled and Tuned by Their Substitution Pattern (Chem. Eur. J. 61/2022) by Biesen, Lukas, Woschko, Dennis, Janiak, Christoph, Müller, Thomas J. J.

    Published in Chemistry : a European journal (02-11-2022)
    “…Aroyl‐S,N‐ketene acetals put a novel, promising class of dyes on the stage of AIEgens. Like a puppet on a string, all their photophysical properties like AIE…”
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    Journal Article
  6. 6

    Retracted: Aggregation‐Induced Emission‐Active Donor‐Substituted Aroyl‐ S , N ‐Ketene Acetals via Nucleophilic Amine Base Attack by Biesen, Lukas, Müller, Thomas J. J.

    Published in ChemPhotoChem (01-11-2023)
    “…Abstract Donor‐substituted aroyl‐ S , N ‐ketene acetals can be rapidly obtained by nucleophilic attack of triethylamine at the acid chloride with concomitant…”
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    Journal Article
  7. 7

    Aroyl‐S,N‐Ketene Acetals: Luminous Renaissance of a Class of Heterocyclic Compounds by Biesen, Lukas, Müller, Thomas J. J.

    Published in Chemistry : a European journal (16-11-2023)
    “…Aroyl‐S,N‐ketene acetals represent a peculiar class of heterocyclic merocyanines, compounds bearing pronounced and rather short dipoles with great push‐pull…”
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  8. 8

    Diaroyl ‐S,N‐ ketene Acetals: Red‐Shifted Solid‐State and Aggregation‐Induced Emitters from a One‐Pot Synthesis by Biesen, Lukas, Hartmann, Yannic, Müller, Thomas J. J.

    Published in Chemistry : a European journal (23-10-2023)
    “…Abstract Symmetric and unsymmetric diaroyl‐ S,N ‐ketene acetals can be readily accessed in consecutive syntheses in good to excellent yields by exploiting the…”
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    Journal Article
  9. 9

    Single molecule aggregation-induced dual and white-light emissive etherified aroyl-,-ketene acetals one-pot synthesis by Biesen, Lukas, Mller, Thomas J. J

    Published in RSC advances (05-06-2023)
    “…Etherified aroyl- S , N -ketene acetals are readily synthesized by a novel one-pot addition-elimination-Williamson-etherification sequence. Although the…”
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    Journal Article
  10. 10

    Solid‐State Emissive Aroyl‐S,N‐Ketene Acetals with Tunable Aggregation‐Induced Emission Characteristics by Biesen, Lukas, Nirmalananthan‐Budau, Nithiya, Hoffmann, Katrin, Resch‐Genger, Ute, Müller, Thomas J. J.

    Published in Angewandte Chemie International Edition (15-06-2020)
    “…N‐Benzyl aroyl‐S,N‐ketene acetals can be readily synthesized by condensation of aroyl chlorides and N‐benzyl 2‐methyl benzothiazolium salts in good to…”
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  11. 11

    Solid‐State Emission and Aggregate Emission of Aroyl‐ S,N‐Ketene Acetals Are Controlled and Tuned by Their Substitution Pattern by Biesen, Lukas, Woschko, Dennis, Janiak, Christoph, Müller, Thomas J. J.

    Published in Chemistry : a European journal (02-11-2022)
    “…Aroyl‐S,N‐ketene acetals are a novel highly diverse class of aggregation‐induced emission fluorogens (AIEgens) with a plethora of interesting properties. An…”
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    Journal Article
  12. 12

    Single molecule aggregation-induced dual and white-light emissive etherified aroyl- S , N -ketene acetals via one-pot synthesis by Biesen, Lukas, Müller, Thomas J J

    Published in RSC advances (05-06-2023)
    “…Etherified aroyl- , -ketene acetals are readily synthesized by a novel one-pot addition-elimination-Williamson-etherification sequence. Although the underlying…”
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    Journal Article
  13. 13

    Asymmetrically bridged aroyl- S , N -ketene acetal-based multichromophores with aggregation-induced tunable emission by Biesen, Lukas, Krenzer, Julius, Nirmalananthan-Budau, Nithiya, Resch-Genger, Ute, Müller, Thomas J J

    Published in Chemical science (Cambridge) (11-05-2022)
    “…Asymmetrically bridged aroyl- , -ketene acetals and aroyl- , -ketene acetal multichromophores can be readily synthesized in consecutive three-, four-, or…”
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    Journal Article
  14. 14

    Diaroyl-S,N-ketene Acetals - Red-Shifted Solid-State and Aggregation-Induced Emitters via One-Pot Synthesis by Biesen, Lukas, Hartmann, Yannic, Müller, Thomas J J

    Published in Chemistry : a European journal (20-07-2023)
    “…Symmetric and unsymmetric diaroyl-S,N-ketene acetals can be readily accessed in consecutive syntheses in good to excellent yields by exploiting the inherent…”
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    Journal Article
  15. 15

    Communication of Bichromophore Emission upon Aggregation – Aroyl‐S,N‐ketene Acetals as Multifunctional Sensor Merocyanines by Biesen, Lukas, May, Lars, Nirmalananthan‐Budau, Nithiya, Hoffmann, Katrin, Resch‐Genger, Ute, Müller, Thomas J. J.

    Published in Chemistry : a European journal (20-09-2021)
    “…Aroyl‐S,N‐ketene acetal‐based bichromophores can be readily synthesized in a consecutive three‐component synthesis in good to excellent yields by condensation…”
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    Journal Article
  16. 16

    Aggregation‐Induced Emission‐Active Donor‐Substituted Aroyl‐S,N‐Ketene Acetals via Nucleophilic Amine Base Attack by Biesen, Lukas, Müller, Thomas J. J.

    Published in ChemPhotoChem (01-11-2023)
    “…Donor‐substituted aroyl‐S,N‐ketene acetals can be rapidly obtained by nucleophilic attack of triethylamine at the acid chloride with concomitant…”
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    Journal Article
  17. 17

    Synthesis and Electronic Properties of Conjugated syn,syn‐Dithienothiazine Donor‐Acceptor‐Donor Dumbbells by Nau, Jennifer, Brüning, Vincent, Biesen, Lukas, Knedel, Tim‐Oliver, Janiak, Christoph, Müller, Thomas J. J.

    Published in European journal of organic chemistry (17-01-2022)
    “…A series of conjugated syn,syn‐dithienothiazine donor‐acceptor‐donor dumbbells is readily synthesized by Suzuki coupling or a one‐pot…”
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  18. 18
  19. 19

    Festkörperemittierende Aroyl‐S,N‐Ketenacetale mit steuerbaren aggregationsinduzierten Emissionseigenschaften by Biesen, Lukas, Nirmalananthan‐Budau, Nithiya, Hoffmann, Katrin, Resch‐Genger, Ute, Müller, Thomas J. J.

    Published in Angewandte Chemie (15-06-2020)
    “…N‐Benzyl‐aroyl‐S,N‐ketenacetale können durch die Kondensation von Aroylchloriden und N‐Benzyl‐2‐methylbenzothiazolium‐Salzen in guten bis ausgezeichneten…”
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  20. 20

    Asymmetrically bridged aroyl-,-ketene acetal-based multichromophores with aggregation-induced tunable emission by Biesen, Lukas, Krenzer, Julius, Nirmalananthan-Budau, Nithiya, Resch-Genger, Ute, Müller, Thomas J. J

    Published in Chemical science (Cambridge) (11-05-2022)
    “…Asymmetrically bridged aroyl- S , N -ketene acetals and aroyl- S , N -ketene acetal multichromophores can be readily synthesized in consecutive three-, four-,…”
    Get full text
    Journal Article