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Sinteza in nekatere pretvorbe organoselenovih spojin
ID Kolarič, Mitja (Author), ID Jereb, Marjan (Mentor) More about this mentor... This link opens in a new window

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Abstract
V sklopu magistrske naloge sem sintetiziral štiriindvajset različnih selenidov in selenoksidov. Najprej sem sintetiziral sedemnajst različnih simetričnih in nesimetričnih selenidov, nato pa sedem izbranih selenidov oksidiral do selenoksidov. V prvem sklopu sem iz aril bromidov in elementarnega selena preko modificirane Grignardove reakcije sintetiziral devet simetričnih selenidov. V drugem sklopu sem pri sobni temperaturi iz difenil diselenida in različnih aktiviranih aromatov pripravil osem nesimetričnih selenidov. Pri teh reakcijah sem kot reagent uporabil Selectfluor$^{TM}$ (F-TEDA) ali PIFA ((bis(trifluoroacetoksi)jodo)benzen). V zadnjem sklopu sem sedem izbranih selenidov oksidiral do selenoksidov z uporabo vodikovega peroksida brez uporabe topil.

Language:Slovenian
Keywords:organoselenove spojine, selenidi, selenoksidi, reakcije pri sobni temperaturi, Selectfluor$^{TM}$, (bis(trifluoroacetoksi)jodo)benzen, reakcije brez topil
Work type:Master's thesis/paper
Typology:2.09 - Master's Thesis
Organization:FKKT - Faculty of Chemistry and Chemical Technology
Year:2025
PID:20.500.12556/RUL-171753 This link opens in a new window
COBISS.SI-ID:249615107 This link opens in a new window
Publication date in RUL:01.09.2025
Views:558
Downloads:145
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Secondary language

Language:English
Title:Synthesis and some conversions of organoselenium compounds
Abstract:
For my master's thesis I have synthesised twenty-four different selenides and selenoxides. First, I synthesised seventeen different symmetrical and unsymmetrical selenides, then I have oxidised seven selected selenides to selenoxides. In the first part I have synthesised nine different symmetrical selenides using aryl bromides and elementary selenium in a modified Grignard reaction. In the second part I have used diphenyl diselenide and various activated aromatic compounds to synthesize eight different unsymmetric selenides at room temperature. In these reactions I have used Selectfluor$^{TM}$ (F-TEDA) or PIFA ((bis(trifluoroacetoxy)iodo)benzene) as a reagent. In the last part I have oxidised seven of the selenides into selenoxides using hydrogen peroxide without the use of solvents.

Keywords:organoselenium compounds, selenides, selenoxides, room temperature reactions, Selectfluor$^{TM}$, (bis(trifluoroacetoxy)iodo)benzene, solvent-free reactions

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