Synthesis of photocleavable protected terminal alkynes for self-assembled monolayers and single molecule electronics
Tekijät
Päivämäärä
2021Pääsyrajoitukset
Tekijä ei ole antanut lupaa avoimeen julkaisuun, joten aineisto on luettavissa vain Jyväskylän yliopiston kirjaston arkistotyöasemalta.
Tekijänoikeudet
Julkaisu on tekijänoikeussäännösten alainen. Teosta voi lukea ja tulostaa henkilökohtaista käyttöä varten. Käyttö kaupallisiin tarkoituksiin on kielletty.
The theoretical part of the thesis introduces self-assembled monolayers, their applications in a view of organic electronics and usage of photocleavable protection groups. Alkanethiol SAMs on gold surface and their surface modifications in a different approach are focused. Theoretical work also contains some information about traditional protection groups and synthesis which are related to the experimental part.
The aim of experimental part was to synthesize a photocleavable protected arylpropiolic acid with an alkanethiol anchoring group and apply it on a gold surface. Prepared monolayer could be used for surface modification and release the terminal alkyne by light activation for further reactions. If experiment could succeed, there is a potential to create a single molecule electronics. As a result, the formation of self-assembled monolayer could not prove via used characterization methods.
Asiasanat
Metadata
Näytä kaikki kuvailutiedotKokoelmat
- Pro gradu -tutkielmat [29561]
Samankaltainen aineisto
Näytetään aineistoja, joilla on samankaltainen nimeke tai asiasanat.
-
Definition of the pnictogen bond (IUPAC Recommendations 2023)
Resnati, Giuseppe; Bryce, David L.; Desiraju, Gautam R.; Frontera, Antonio; Krossing, Ingo; Legon, Anthony C.; Metrangolo, Pierangelo; Nicotra, Francesco; Rissanen, Kari; Scheiner, Steve; Terraneo, Giancarlo (De Gruyter, 2024)This recommendation proposes a definition for the term “pnictogen bond”; the term pnictogen bond designates a subset of the attractive interactions between an electrophilic region on a pnictogen atom in a molecular entity ... -
Exploring the self-assembly of resorcinarenes : from molecular level interactions to mesoscopic structures
Helttunen, Kaisa (University of Jyväskylä, 2012) -
Synthesis, characterization, and reactivity of heavier group 13 and 14 metallylenes and metalloid clusters : small molecule activation and more
Vasko, Petra (University of Jyväskylä, 2015) -
Subcomponent self‐assembly of a cyclic tetranuclear Fe(II) helicate in a highly diastereoselective self‐sorting manner
Anhäuser, Jana; Puttreddy, Rakesh; Glanz, Lukas; Schneider, Andreas; Engeser, Marianne; Rissanen, Kari; Lützen, Arne (Wiley-VCH Verlag, 2019)An enantiomerically pure diamine based on the 4,15‐difunctionalized [2.2]paracyclophane scaffold and 2‐formylpyridine self‐assemble into an optically pure cyclic metallosupramolecular Fe₄L₆ helicate upon mixing with iron(II) ... -
Mechanochemically driven covalent self-assembly of a chiral mono-biotinylated hemicucurbit[8]uril
Suut-Tuule, Elina; Jarg, Tatsiana; Tikker, Priit; Lootus, Ketren-Marlein; Martõnova, Jevgenija; Reitalu, Rauno; Ustrnul, Lukas; Ward, Jas S.; Rjabovs, Vitalijs; Shubin, Kirill; Nallaparaju, Jagadeesh V.; Vendelin, Marko; Preis, Sergei; Öeren, Mario; Rissanen, Kari; Kananovich, Dzmitry; Aav, Riina (Elsevier, 2024)Solution-based synthesis of complex molecules with high efficiency leverages supramolecular control over covalent bond formation. Herein, we present the mechanosynthesis of chiral mono-biotinylated hemicucurbit[8]urils ...
Ellei toisin mainittu, julkisesti saatavilla olevia JYX-metatietoja (poislukien tiivistelmät) saa vapaasti uudelleenkäyttää CC0-lisenssillä.