The photocatalytic conversion of CO_(2)into solar‐powered fuels is viewed as a forward‐looking strategy to address energy scarcity and global warming.This work demonstrated the selective photoreduction of CO_(2)to C...The photocatalytic conversion of CO_(2)into solar‐powered fuels is viewed as a forward‐looking strategy to address energy scarcity and global warming.This work demonstrated the selective photoreduction of CO_(2)to CO using ultrathin Bi_(12)O_(17)Cl_(2)nanosheets decorated with hydrothermally synthesized bismuth clusters and oxygen vacancies(OVs).The characterizations revealed that the coexistences of OVs and Bi clusters generated in situ contributed to the high efficiency of CO_(2)–CO conversion(64.3μmol g^(−1)h^(−1))and perfect selectivity.The OVs on the facet(001)of the ultrathin Bi_(12)O_(17)Cl_(2)nanosheets serve as sites for CO_(2)adsorption and activation sites,capturing photoexcited electrons and prolonging light absorption due to defect states.In addition,the Bi‐cluster generated in situ offers the ability to trap holes and the surface plasmonic resonance effect.This study offers great potential for the construction of semiconductor hybrids as multiphotocatalysts,capable of being used for the elimination and conversion of CO_(2)in terms of energy and environment.展开更多
New chiral C_2-symmetrical bis(oxazoline) compounds bearing one isobutyl-, secbutyl-, benzyl- or isopropyl-substituent at the 4-position have been prepared and characterized.
The synthesis of bis(oxazoline) dicarboxylate derivatives was investigated. Diethyl-aminosulfur trifluoride (DAST) was used as a convenient cyclization reagent in the synthesis of bis(oxazoline) dicarboxylate derivati...The synthesis of bis(oxazoline) dicarboxylate derivatives was investigated. Diethyl-aminosulfur trifluoride (DAST) was used as a convenient cyclization reagent in the synthesis of bis(oxazoline) dicarboxylate derivatives, which can not be obtained by the general method using MsCl and Et3N as dehydrating cyclization reagent.展开更多
The mass spectrometric fragmentation of 1,8-bis [ 4-substituted （oxazolin-2-yl） ] anthracenes （AnBOXes） was investigated by using mass-analyzed ion kinetic energy spectrometry under electron-impact ionization cond...The mass spectrometric fragmentation of 1,8-bis [ 4-substituted （oxazolin-2-yl） ] anthracenes （AnBOXes） was investigated by using mass-analyzed ion kinetic energy spectrometry under electron-impact ionization conditions. All the compounds could undergo a ring contraction by the loss of an RCH = CH2 molecule to form 1-oxazirinyl-8-（oxazolin- 2-yl） anthracene ions, which could further lose an R radical, followed by the loss of oxazoline. These ions could also eliminate an R radical and subsequently undergo ring-contraction rearrangements to lose a CHCH2O fragraent and an epoxide molecule, respectively. The ions that are formed could further lose CHCH2O and CH2 = CH fragments. Several ring-contraction rearrangements of the oxazoline ring were observed under electron-impact ionization conditions.展开更多
基金Natural Science Foundation of Shandong Province,Grant/Award Number:ZR2022MB106national training program of innovation and entrepreneurship for undergraduates,Grant/Award Number:202210424099National Natural Science Foundation of China,Grant/Award Numbers:21601067,21701057,21905147。
文摘The photocatalytic conversion of CO_(2)into solar‐powered fuels is viewed as a forward‐looking strategy to address energy scarcity and global warming.This work demonstrated the selective photoreduction of CO_(2)to CO using ultrathin Bi_(12)O_(17)Cl_(2)nanosheets decorated with hydrothermally synthesized bismuth clusters and oxygen vacancies(OVs).The characterizations revealed that the coexistences of OVs and Bi clusters generated in situ contributed to the high efficiency of CO_(2)–CO conversion(64.3μmol g^(−1)h^(−1))and perfect selectivity.The OVs on the facet(001)of the ultrathin Bi_(12)O_(17)Cl_(2)nanosheets serve as sites for CO_(2)adsorption and activation sites,capturing photoexcited electrons and prolonging light absorption due to defect states.In addition,the Bi‐cluster generated in situ offers the ability to trap holes and the surface plasmonic resonance effect.This study offers great potential for the construction of semiconductor hybrids as multiphotocatalysts,capable of being used for the elimination and conversion of CO_(2)in terms of energy and environment.
基金the Foundation for Academic Leader by the Education Department of Hunan province.
文摘New chiral C_2-symmetrical bis(oxazoline) compounds bearing one isobutyl-, secbutyl-, benzyl- or isopropyl-substituent at the 4-position have been prepared and characterized.
文摘The synthesis of bis(oxazoline) dicarboxylate derivatives was investigated. Diethyl-aminosulfur trifluoride (DAST) was used as a convenient cyclization reagent in the synthesis of bis(oxazoline) dicarboxylate derivatives, which can not be obtained by the general method using MsCl and Et3N as dehydrating cyclization reagent.
基金Supported by the National Natural Science Foundation of China(No. 20272002).
文摘The mass spectrometric fragmentation of 1,8-bis [ 4-substituted （oxazolin-2-yl） ] anthracenes （AnBOXes） was investigated by using mass-analyzed ion kinetic energy spectrometry under electron-impact ionization conditions. All the compounds could undergo a ring contraction by the loss of an RCH = CH2 molecule to form 1-oxazirinyl-8-（oxazolin- 2-yl） anthracene ions, which could further lose an R radical, followed by the loss of oxazoline. These ions could also eliminate an R radical and subsequently undergo ring-contraction rearrangements to lose a CHCH2O fragraent and an epoxide molecule, respectively. The ions that are formed could further lose CHCH2O and CH2 = CH fragments. Several ring-contraction rearrangements of the oxazoline ring were observed under electron-impact ionization conditions.
