Ester compound
US-2024025838-A1 · Jan 25, 2024 · US
US9537110B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9537110-B2 |
| Application number | US-201314378684-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 20, 2013 |
| Priority date | Feb 22, 2012 |
| Publication date | Jan 3, 2017 |
| Grant date | Jan 3, 2017 |
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An organic compound represented by formula (1) or formula (2) that is easy to synthesize, and has excellent chemical stability, semiconductor characteristics (high carrier mobility) and high solubility in a solvent. in formula (1), X is oxygen, sulfur or selenium; n is 0 or 1; R 1 to R 3 are hydrogen, fluorine, alkyl having 1 to 20 carbons, aryl, pyridyl, furyl, thienyl, thiazolyl or the like. However, except for a case where X is selenium, a case where all of R 1 to R 3 are simultaneously hydrogen is excluded, and a case where X is sulfur and all of R 1 are simultaneously butyl is also excluded. In formula (2), X is oxygen, sulfur or selenium; n is 0 or 1; R 1 to R 2 are hydrogen, alkyl having 1 to 20 carbons, aryl, pyridyl, furyl, thienyl, thiazolyl or the like; however, a case where all of R 1 to R 2 are simultaneously hydrogen is excluded.
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What is claimed is: 1. A compound of formula (1-1) or formula (1-2): wherein, in formula (1-1) and formula (1-2), X is oxygen, sulfur or selenium; each n is independently 0 or 1; each R 3 is independently fluorine, alkyl having 1 to 20 carbons, aryl, pyridyl, furyl, thienyl or thiazolyl, optionally one or more hydrogens in the alkyl is replaced by fluorine, and optionally one or more hydrogens on a ring of the aryl, the pyridyl, the furyl, the thienyl and the thiazolyl is replaced by at least one selected from the group consisting of halogen and alkyl having 1 to 10 carbons. 2. The compound according to claim 1 , wherein R 3 in formula (1-1) and formula (1-2) is an identical group selected from the group consisting of alkyl having 4 to 15 carbons, phenyl, furyl and thienyl. 3. A method for manufacturing the compound according to claim 1 , wherein, X is sulfur or selenium, comprising: a step for allowing coupling of compounds of formula (11) to obtain a compound of formula (12); a step for allowing deprotection of methoxy of the compound of formula (12) to obtain a compound of formula (13); a step for allowing the compound of formula (13) to react with N,N-dialkyl thiocarbamoyl chloride or N,N-dialkyl selenocarbamoyl chloride to obtain a compound of formula (14); and a step for heating the compound of formula (14) to obtain a compound of formula (15): wherein, in formulas (11) to (15), X is sulfur or selenium, n and R 1 to R 3 each are defined in a manner identical with the definitions of an identical symbol in formula (1), Me is methyl, and in formula (14), R's are each independently alkyl having 1 to 3 carbons. 4. A method for manufacturing the compound according to claim 1 , wherein, X is selenium, comprising: a step for allowing coupling of compounds of formula (11) to obtain a compound of formula (12); a step for allowing deprotection of methoxy of the compound of formula (12) to obtain a compound of formula (13); a step for allowing the compound of formula (13) to react with trifluoromethanesulfonyl chloride or trifluoromethanesulfonic anhydride to obtain a compound of formula (16); a step for allowing coupling of the compounds of formula (16) with boranes to obtain boronic ester of formula (17); a step for brominating the boronic ester of formula (17) with copper bromide to obtain a compound of formula (18); and a step for lithiating the compound of formula (18), and then allowing the resulting product to react with selenium chloride to obtain a compound of formula (15): wherein, in formulas (11) to (13) and formulas (15) to (18), X is selenium, n and R 1 to R 3 each are defined in a manner identical with the definitions of an identical symbol in formula (1), Me is methyl, and in formula (17), R's are each independently alkyl having 1 to 3 carbons. 5. A method for manufacturing the compound according to claim 1 , wherein, X is oxygen, comprising: a step for allowing coupling of compounds of formula (11) to obtain a compound of formula (12); a step for allowing deprotection of methoxy of the compound of formula (12) to obtain a compound of formula (13); a step for heating and dehydrating the compound of formula (13) under a zeolite catalyst to obtain a compound of formula (15): wherein, in formulas (11) to (13) and (15), X is oxygen, n and R 1 to R 3 each are defined in a manner identical with the definitions of an identical symbol in formula (1), and Me is methyl. 6. An organic semiconductor material, composed of the compound according to claim 1 . 7. An organic semiconductor film, including the organic semiconductor material according to claim 6 . 8. An organic field effect transistor comprising a substrate, a gate electrode, a gate insulating film, a source electrode, a drain electrode and an organic semiconductor layer, wherein the organic semiconductor layer is constituted of the organic semiconductor film according to claim 7 .
containing three or more hetero rings · CPC title
ortho- or peri-condensed with carbocyclic rings or ring systems · CPC title
condensed with carbocyclic rings or ring systems · CPC title
Heterocyclic compounds containing rings having selenium or tellurium atoms as the only ring hetero atoms · CPC title
containing three or more hetero rings · CPC title
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