Matti Haukka
Contact search available for JYU staff members.
Active JYU affiliations
- Department of Chemistry, Professor
Research interests
The goal of EMS-group is to produce new type of materials by linking simple compounds into polymeric structures. The aim is to produce conductive, optically active and catalytically active materials as well as materials suitable for recovering and recycling metals.
Projects as Principal investigator
- Chemically Active 3D Printed Devices
- Academy of Finland
- Functional Metallopolymers
- Academy of Finland
- Metallien talteenottoon soveltuvat 3D-tulostusmateriaalit
- Technology Industries of Finland Centennial Foundation
Publications
1 of 10
- Classics Meet Classics : Theoretical and Experimental Studies of Halogen Bonding in Adducts of Platinum(II) 1,5-Cyclooctadiene Halide Complexes with Diiodine, Iodoform, and 1,4-Diiodotetrafluorobenzene (2021) Bulatova, Margarita; et al.; A1
- Considering lithium-ion battery 3D-printing via thermoplastic material extrusion and polymer powder bed fusion (2021) Maurel, Alexis; et al.; A1; OA
- Reaction mechanism of regioisomerization in binuclear (diaminocarbene)PdII complexes (2021) Mikherdov, Alexander S.; et al.; A1
- Synthesis, X-Ray Structure, Tautomerism Aspect, and Chemical Insight of The 3-(1H-Indol-2-yl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-6-ol (2021) Boraei, Ahmed T.A.; et al.; A1
- The Se∙∙∙Hal halogen bonding : co-crystals of selenoureas with fluorinated organohalides (2021) Chernysheva, Maria V.; et al.; A1
- The S … Hal and Se … Hal chalcogen bonding in a series of thiourea, selenourea and their derivatives (2021) Chernysheva, Maria V.; et al.; A1; OA
- X-ray Crystal Structure and Hirshfeld Analysis of Gem-Aminals-Based Morpholine, Pyrrolidine, and Piperidine Moieties (2021) Al-Majid, Abdullah Mohammed; et al.; A1; OA
- X-Ray structure, Hirshfeld analysis and DFT studies of two new hits of triazolyl-indole bearing alkylsulfanyl moieties (2021) Boraei, Ahmed T.A.; et al.; A1; OA
- 3D Printed Palladium Catalyst for Suzuki-Miyaura Cross-coupling Reactions (2020) Haukka, Matti; et al.; A1; OA
- Angular Regioselectivity in the Reactions of 2-Thioxopyrimidin-4-ones and Hydrazonoyl Chlorides : Synthesis of Novel Stereoisomeric Octahydro[1,2,4]triazolo[4,3-a]quinazolin-5-ones (2020) Said, Awad I.; et al.; A1; OA
- A Novel Halogen Bond Acceptor : 1-(4-Pyridyl)-4-Thiopyridine (PTP) Zwitterion (2020) Ding, Xin; et al.; A1; OA
- A novel synthetic approach to pyran-2,4-dione scaffold production : microwave-assisted dimerization, cyclization, and expeditious regioselective conversion into β-enamino-pyran-2,4-diones (2020) Sarhan, Ahmed A.M.; et al.; A1; OA
- Asymmetric hydrogenation of an α-unsaturated carboxylic acid catalyzed by intact chiral transition metal carbonyl cluster : diastereomeric control of enantioselectivity (2020) Abdel-Magied, Ahmed F.; et al.; A1; OA
- Attractive halogen···halogen interactions in crystal structure of trans-dibromogold(III) complex (2020) Tskhovrebov, Alexander G.; et al.; A1
- Cis- and trans molybdenum oxo complexes of a prochiral tetradentate aminophenolate ligand : Synthesis, characterization and oxotransfer activity (2020) Hossain, Md Kamal; et al.; A1; OA
- C,N-chelated diaminocarbene platinum(II) complexes derived from 3,4-diaryl-1H-pyrrol-2,5-diimines and cis-dichlorobis(isonitrile)platinum(II): Synthesis, cytotoxicity, and catalytic activity in hydrosilylation reactions (2020) Afanasenko, Anastasiia M.; et al.; A1; OA
- Design, Construction, and Characterization of a New Regioisomer and Diastereomer Material Based on the Spirooxindole Scaffold Incorporating a Sulphone Function (2020) Al-Majid, Abdullah M.; et al.; A1; OA
- Diversity-Oriented Stereocontrolled Synthesis of Some Piperidine- and Azepane-Based Fluorine-Containing β-Amino Acid Derivatives (2020) Kiss, Loránd; et al.; A1
- Halogen Bonding Involving Palladium(II) as an XB Acceptor (2020) Katlenok, Eugene A.; et al.; A1
- Influence of substituents in aromatic ring on the strength of halogen bonding in iodobenzene derivatives (2020) Chernysheva, Maria V.; et al.; A1; OA
