The chromogenic responding ability increases as the substituent changes from phenyl to naphthyl or anthryl.

实验结果表明，偶氮基团的引入改善了8-羟基喹啉的力，并且在乙腈溶液中随着取代基由苯基变为萘基和蒽基时，化合物的吸收光谱发红移。

P-methoxybenzeneacetonitrile was prepared in 34. 8% yield starting from anisole, via chloromethylation, cyanogenation and fractional distillation.

苯甲醚为原料,经过氯甲基化,氰化反应后,通过精馏获对甲氧基苯乙腈,总收率为34.8%。

Microspheric trans aconitic acid imprinted polymers were synthesized via a precipitation polymerization with acetonitrile as dispersion solvent.

乙腈为分散,采用沉淀聚合法合成了反乌头酸分子印迹聚合物微球。

Alkylation of Phenylacetonitrile was realized from phenylacetonitrile and benzyl chloride by using PS-PEG-400 as triphase phase transfer catalyst.

摘要利用固载化聚乙二醇-400作三相相转移催化，氧化钾的水溶液作碱，从苯乙腈和苄基氯出发合成了苯乙腈的单烷基化物-α-苄基苯乙腈。

In the presence of ethanonitrile and polyethylene glycol, anthrone reacts with ammonium ceric nitrate to form 1 nitroanthraquinone.

在乙腈、相转移催化聚乙二醇存在下 ,蒽酮与硝酸铈铵反应成 1 -硝基蒽醌。

Calcium ammine catalyst was prepared with metal calcium,dehydrated liquid ammonia as raw materials,nano-silica as a carrier and acetonitrile and propylene epoxide as modifiers.

采用金属钙、脱水液氨、载体纳米二氧化硅及改性乙腈与环氧丙烷制备出氨钙体系催化。

The chromogenic responding ability increases as the substituent changes from phenyl to naphthyl or anthryl.

实验结果表明，偶氮基团的引入改善了8-羟基喹啉的生色能力，并且在乙腈溶液中随着取代基由苯基变为萘基和蒽基时，的吸收光谱发生红移。

P-methoxybenzeneacetonitrile was prepared in 34. 8% yield starting from anisole, via chloromethylation, cyanogenation and fractional distillation.

以苯甲醚为原料,经过氯甲基,氰反应后,通过精馏获对甲氧基苯乙腈,总收率为34.8%。

Microspheric trans aconitic acid imprinted polymers were synthesized via a precipitation polymerization with acetonitrile as dispersion solvent.

以乙腈为散剂,采用沉淀聚法成了反乌头酸迹聚微球。

Alkylation of Phenylacetonitrile was realized from phenylacetonitrile and benzyl chloride by using PS-PEG-400 as triphase phase transfer catalyst.

摘要利用固载聚乙二醇-400作三相相转移催剂，以氢氧钾的水溶液作碱，从苯乙腈和苄基氯出发成了苯乙腈的单烷基-α-苄基苯乙腈。

In the presence of ethanonitrile and polyethylene glycol, anthrone reacts with ammonium ceric nitrate to form 1 nitroanthraquinone.

在乙腈、相转移催剂聚乙二醇存在下 ,蒽酮与硝酸铈铵反应生成 1 -硝基蒽醌。

Calcium ammine catalyst was prepared with metal calcium,dehydrated liquid ammonia as raw materials,nano-silica as a carrier and acetonitrile and propylene epoxide as modifiers.

采用金属钙、脱水液氨、载体纳米二氧硅及改性剂乙腈与环氧丙烷制备出氨钙体系催剂。

The chromogenic responding ability increases as the substituent changes from phenyl to naphthyl or anthryl.

实验结果表明，偶氮基团的引入8-羟基喹啉的生色能力，并且在乙腈中随着取代基由苯基变为萘基和蒽基时，化合物的吸收光谱发生红移。

P-methoxybenzeneacetonitrile was prepared in 34. 8% yield starting from anisole, via chloromethylation, cyanogenation and fractional distillation.

以苯甲醚为原料,经过氯甲基化,氰化反应后,通过精馏获对甲氧基苯乙腈,总收率为34.8%。

Microspheric trans aconitic acid imprinted polymers were synthesized via a precipitation polymerization with acetonitrile as dispersion solvent.

以乙腈为分散剂,采用沉淀聚合法合成反乌头酸分子印迹聚合物微球。

Alkylation of Phenylacetonitrile was realized from phenylacetonitrile and benzyl chloride by using PS-PEG-400 as triphase phase transfer catalyst.

摘要利用固载化聚乙二醇-400三相相转移催化剂，以氢氧化钾的水碱，从苯乙腈和苄基氯出发合成苯乙腈的单烷基化物-α-苄基苯乙腈。

In the presence of ethanonitrile and polyethylene glycol, anthrone reacts with ammonium ceric nitrate to form 1 nitroanthraquinone.

在乙腈、相转移催化剂聚乙二醇存在下 ,蒽酮与硝酸铈铵反应生成 1 -硝基蒽醌。

Calcium ammine catalyst was prepared with metal calcium,dehydrated liquid ammonia as raw materials,nano-silica as a carrier and acetonitrile and propylene epoxide as modifiers.

采用金属钙、脱水氨、载体纳米二氧化硅及性剂乙腈与环氧丙烷制备出氨钙体系催化剂。

The chromogenic responding ability increases as the substituent changes from phenyl to naphthyl or anthryl.

实验结果表明，偶氮基团引入改善了8-羟基喹啉生色能力，并且在溶液中随着取代基由苯基变为萘基和蒽基时，化合物吸收光谱发生红移。

P-methoxybenzeneacetonitrile was prepared in 34. 8% yield starting from anisole, via chloromethylation, cyanogenation and fractional distillation.

以苯甲醚为原料,经过氯甲基化,氰化反应后,通过精馏获对甲氧基苯,总收率为34.8%。

Microspheric trans aconitic acid imprinted polymers were synthesized via a precipitation polymerization with acetonitrile as dispersion solvent.

以为分散剂,采用沉淀聚合法合成了反乌头酸分子印迹聚合物微球。

Alkylation of Phenylacetonitrile was realized from phenylacetonitrile and benzyl chloride by using PS-PEG-400 as triphase phase transfer catalyst.

摘要利用固载化聚二醇-400作三相相转移催化剂，以氢氧化钾水溶液作碱，从苯和苄基氯出发合成了苯单烷基化物-α-苄基苯。

In the presence of ethanonitrile and polyethylene glycol, anthrone reacts with ammonium ceric nitrate to form 1 nitroanthraquinone.

在、相转移催化剂聚二醇存在下 ,蒽酮与硝酸铈铵反应生成 1 -硝基蒽醌。

Calcium ammine catalyst was prepared with metal calcium,dehydrated liquid ammonia as raw materials,nano-silica as a carrier and acetonitrile and propylene epoxide as modifiers.

采用金属钙、脱水液氨、载体纳米二氧化硅及改性剂与环氧丙烷制备出氨钙体系催化剂。

The chromogenic responding ability increases as the substituent changes from phenyl to naphthyl or anthryl.

实验结果表明，偶氮基团的引入改善了8-羟基喹啉的生色能力，并且在溶液中随着取代基由基变为萘基和蒽基时，化合物的吸收光谱发生红移。

P-methoxybenzeneacetonitrile was prepared in 34. 8% yield starting from anisole, via chloromethylation, cyanogenation and fractional distillation.

以甲醚为原料,经过氯甲基化,氰化反应后,通过精馏获对甲氧基,总收率为34.8%。

Microspheric trans aconitic acid imprinted polymers were synthesized via a precipitation polymerization with acetonitrile as dispersion solvent.

以为分散剂,采用沉淀聚合法合成了反乌头酸分子印迹聚合物微球。

Alkylation of Phenylacetonitrile was realized from phenylacetonitrile and benzyl chloride by using PS-PEG-400 as triphase phase transfer catalyst.

摘要利用固载化聚二醇-400作三相相转移催化剂，以氢氧化钾的水溶液作碱，从和苄基氯出发合成了的单烷基化物-α-苄基。

In the presence of ethanonitrile and polyethylene glycol, anthrone reacts with ammonium ceric nitrate to form 1 nitroanthraquinone.

在、相转移催化剂聚二醇存在下 ,蒽酮与硝酸铈铵反应生成 1 -硝基蒽醌。

Calcium ammine catalyst was prepared with metal calcium,dehydrated liquid ammonia as raw materials,nano-silica as a carrier and acetonitrile and propylene epoxide as modifiers.

采用金属钙、脱水液氨、载体纳米二氧化硅及改性剂与环氧丙烷制备出氨钙体系催化剂。

The chromogenic responding ability increases as the substituent changes from phenyl to naphthyl or anthryl.

实验结果表明，偶氮基团的引入改善了8-羟基喹啉的生色能力，并且在溶液中随着取代基由基变为萘基和蒽基时，化合物的吸收光谱发生红移。

P-methoxybenzeneacetonitrile was prepared in 34. 8% yield starting from anisole, via chloromethylation, cyanogenation and fractional distillation.

以甲醚为原料,经过氯甲基化,氰化反,过精馏获对甲氧基,总收率为34.8%。

Microspheric trans aconitic acid imprinted polymers were synthesized via a precipitation polymerization with acetonitrile as dispersion solvent.

以为分散剂,采用沉淀聚合法合成了反乌头酸分子印迹聚合物微球。

Alkylation of Phenylacetonitrile was realized from phenylacetonitrile and benzyl chloride by using PS-PEG-400 as triphase phase transfer catalyst.

摘要利用固载化聚二醇-400作三相相转移催化剂，以氢氧化钾的水溶液作碱，从和苄基氯出发合成了的单烷基化物-α-苄基。

In the presence of ethanonitrile and polyethylene glycol, anthrone reacts with ammonium ceric nitrate to form 1 nitroanthraquinone.

在、相转移催化剂聚二醇存在下 ,蒽酮与硝酸铈铵反生成 1 -硝基蒽醌。

Calcium ammine catalyst was prepared with metal calcium,dehydrated liquid ammonia as raw materials,nano-silica as a carrier and acetonitrile and propylene epoxide as modifiers.

采用金属钙、脱水液氨、载体纳米二氧化硅及改性剂与环氧丙烷制备出氨钙体系催化剂。

The chromogenic responding ability increases as the substituent changes from phenyl to naphthyl or anthryl.

实验结果表明，偶氮基团改善了8-羟基喹啉生色能力，并且在乙腈溶液中随着取代基由基变为萘基和蒽基时，化合物吸收光谱发生红移。

P-methoxybenzeneacetonitrile was prepared in 34. 8% yield starting from anisole, via chloromethylation, cyanogenation and fractional distillation.

以甲醚为原料,经过氯甲基化,氰化反应后,通过精馏获对甲氧基乙腈,总收率为34.8%。

Microspheric trans aconitic acid imprinted polymers were synthesized via a precipitation polymerization with acetonitrile as dispersion solvent.

以乙腈为分散剂,采用沉淀聚合法合成了反乌头酸分子印迹聚合物微球。

Alkylation of Phenylacetonitrile was realized from phenylacetonitrile and benzyl chloride by using PS-PEG-400 as triphase phase transfer catalyst.

摘要利用固载化聚乙二醇-400作三相相转移催化剂，以氢氧化钾水溶液作，乙腈和苄基氯出发合成了乙腈单烷基化物-α-苄基乙腈。

In the presence of ethanonitrile and polyethylene glycol, anthrone reacts with ammonium ceric nitrate to form 1 nitroanthraquinone.

在乙腈、相转移催化剂聚乙二醇存在下 ,蒽酮与硝酸铈铵反应生成 1 -硝基蒽醌。

Calcium ammine catalyst was prepared with metal calcium,dehydrated liquid ammonia as raw materials,nano-silica as a carrier and acetonitrile and propylene epoxide as modifiers.

采用金属钙、脱水液氨、载体纳米二氧化硅及改性剂乙腈与环氧丙烷制备出氨钙体系催化剂。

The chromogenic responding ability increases as the substituent changes from phenyl to naphthyl or anthryl.

实验结果表明，偶氮引入改善了8-羟喹啉生色能力，并且在溶液中随着取代由变为萘和蒽时，化合物吸收光谱发生红移。

P-methoxybenzeneacetonitrile was prepared in 34. 8% yield starting from anisole, via chloromethylation, cyanogenation and fractional distillation.

以甲醚为原料,经过氯甲化,氰化反应后,通过精馏获对甲氧,总收率为34.8%。

Microspheric trans aconitic acid imprinted polymers were synthesized via a precipitation polymerization with acetonitrile as dispersion solvent.

以为分散剂,采用沉淀聚合法合成了反乌头酸分子印迹聚合物微球。

Alkylation of Phenylacetonitrile was realized from phenylacetonitrile and benzyl chloride by using PS-PEG-400 as triphase phase transfer catalyst.

摘要利用固载化聚二醇-400作三相相转移催化剂，以氢氧化钾水溶液作碱，从和苄氯出发合成了单烷化物-α-苄。

In the presence of ethanonitrile and polyethylene glycol, anthrone reacts with ammonium ceric nitrate to form 1 nitroanthraquinone.

在、相转移催化剂聚二醇存在下 ,蒽酮与硝酸铈铵反应生成 1 -硝蒽醌。

Calcium ammine catalyst was prepared with metal calcium,dehydrated liquid ammonia as raw materials,nano-silica as a carrier and acetonitrile and propylene epoxide as modifiers.

采用金属钙、脱水液氨、载体纳米二氧化硅及改性剂与环氧丙烷制备出氨钙体系催化剂。

The chromogenic responding ability increases as the substituent changes from phenyl to naphthyl or anthryl.

实验结果表明，偶氮基团的引入改善了8-羟基喹啉的生色能力，并且在乙腈溶液中随着取代基由苯基变为萘基和蒽基，物的吸收光谱发生红移。

P-methoxybenzeneacetonitrile was prepared in 34. 8% yield starting from anisole, via chloromethylation, cyanogenation and fractional distillation.

以苯甲醚为原料,经过氯甲基,氰反应后,通过精馏获对甲氧基苯乙腈,总收率为34.8%。

Microspheric trans aconitic acid imprinted polymers were synthesized via a precipitation polymerization with acetonitrile as dispersion solvent.

以乙腈为分散剂,采用沉淀聚法成了反乌头酸分聚物微球。

Alkylation of Phenylacetonitrile was realized from phenylacetonitrile and benzyl chloride by using PS-PEG-400 as triphase phase transfer catalyst.

摘要利用固载聚乙二醇-400作三相相转移催剂，以氢氧钾的水溶液作碱，从苯乙腈和苄基氯出发成了苯乙腈的单烷基物-α-苄基苯乙腈。

In the presence of ethanonitrile and polyethylene glycol, anthrone reacts with ammonium ceric nitrate to form 1 nitroanthraquinone.

在乙腈、相转移催剂聚乙二醇存在下 ,蒽酮与硝酸铈铵反应生成 1 -硝基蒽醌。

Calcium ammine catalyst was prepared with metal calcium,dehydrated liquid ammonia as raw materials,nano-silica as a carrier and acetonitrile and propylene epoxide as modifiers.

采用金属钙、脱水液氨、载体纳米二氧硅及改性剂乙腈与环氧丙烷制备出氨钙体系催剂。