prof. dr hab. inż. Dariusz Witt | Politechnika Gdańska

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prof. dr hab. inż. Dariusz Witt

Kontakt:

email:
chemwitt@pg.edu.pl
strona:
https://mostwiedzy.pl/dariusz-witt,8859-1

Zajmowane stanowiska:

Profesor

miejsce pracy:
Katedra Chemii Organicznej
Budynek A Wydziału Chemicznego pokój 105
telefon:
(58) 347 18 51
prof. dr hab. inż. Dariusz Witt

Publikacje:

  1. In the present work, we report the development of a rapid, efcient, and solvent-free procedure for the N-methylation of secondary amines under mechanochemical conditions. After optimization of the milling parameters, a vibrational ball mill was used to synthesize 26 tertiary N-methylated amine derivatives in a short time of 20 min (30 Hz frequency) and high yields ranging from 78 to 95%. An exception was compounds having a hydroxyl...

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  2. Publikacja
    • A. Lindstaedt
    • J. Doroszuk
    • A. Machnikowska
    • A. Dziadosz
    • P. Barski
    • V. Raffa
    • D. Witt

    - Materials - Rok 2024

    We developed a fluorescent molecular probe based on gold nanoparticles functionalized with N,N′-bis(2-(1-piperazino)ethyl)-3,4,9,10-perylenetetracarboxylic acid diimide dihydrochloride, and these probes exhibit potential for applications in microscopic thermometry. The intensity of fluorescence was affected by changes in temperature. Chemical environments, such as different buffers with the same pH, also resulted in different fluorescence...

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  3. The simple, convenient, and efficient methods for the preparation of unsymmetrical vinyl disulfides with additional functional groups under mild conditions with moderate to high yields were designed. The developed methods include the reaction of S-vinyl phosphorodithioate with thiotosylates or S-vinyl thiotosylate with thiols. The designed methods allow for the synthesis of unsymmetrical vinyl disulfides with additional functionalities...

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  4. A simple, efficient, and practical sulfenylation at the C2 position of N-tosylindoles under mild conditions was developed. The designed transformation is based on the reaction of N-tosylindoles with BuLi and S-alkyl, and S-aryl phosphorodithioates or thiotosylates to produce 2-sulfenylindoles in moderate to high yields. The presence of additional hydroxy, carboxy, or amino functionalities did not disturb the formation of products

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  5. We developed a simple and efficient method for the synthesis of functionalized unsymmetrical Z‐alkenyl disulfides under mild conditions in moderate to good yields. The designed method is based on the reaction of α‐thiophosphorylated carbonyl compounds with thiotosylates in the presence of a base. The developed method allows the preparation of unsymmetrical Z‐alkenyl disulfides bearing additional hydroxy, carboxy, or ester functionalities

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