Compared with diolefine rubber,EPDM has less double bond.

烯烃橡胶相比,EPDM的双键很少。

Ring closing metathesis (RCM) of dienes to cycloalkene provides an important tool for C-C double bond formation catalyzed by metal carbene.

关转换反应是形成碳碳双键的重要反应之一,即双烯化合在金属碳烯催化下关得到烯类化合。

Ethyl phenylacrylate intermediate bringing a double bond was introduced first,which is subsequently transformed into triketone and then DCM was obtained with high purity.

采用具有烯烃架的β-苯基丙烯酸酯为间体先引入双键,再经过三酮合制备乙烯基吡喃。

Results indicate interestingly that the double bond of GMA polymerized with polystyryl carbanion and the molar ratio of epoxy end group and polystyrene oligomer can be adjusted.

在GMA聚苯乙烯阴离子反应的过程，GMA在活性种的终端发生了聚合，所得产氧端基聚合产的摩尔比可根据需要进行调节。

Interestingly, in spite of its instability, the O3 molecule can be stabilized as an ozonide between the double bonds of a monounsaturated fatty acid such as oleic acid.

有趣的是，尽管不稳定，超氧O3分子却能以双键结合安定于像油酸那样的单元不饱和脂肪酸形成超氧O3化。

Compared with diolefine rubber,EPDM has less double bond.

与二烯烃橡胶相比,EPDM的双键很少。

Ring closing metathesis (RCM) of dienes to cycloalkene provides an important tool for C-C double bond formation catalyzed by metal carbene.

关转换反应是形成碳碳双键的重要反应之一,即双烯化合物在金属碳烯催化下关得到烯类化合物。

Ethyl phenylacrylate intermediate bringing a double bond was introduced first,which is subsequently transformed into triketone and then DCM was obtained with high purity.

采用具有烯烃架的β-苯基丙烯酸酯为中间体先引入双键,再经过三酮合制备乙烯基吡喃。

Results indicate interestingly that the double bond of GMA polymerized with polystyryl carbanion and the molar ratio of epoxy end group and polystyrene oligomer can be adjusted.

在GMA与聚苯乙烯阴离子反应的过程中，GMA在活性种的终发生了聚合，所得产物中基与聚合产物的摩尔比可根据需要进行调节。

Interestingly, in spite of its instability, the O3 molecule can be stabilized as an ozonide between the double bonds of a monounsaturated fatty acid such as oleic acid.

有趣的是，尽管不稳定，超O3分子却能以双键结合安定于像油酸那样的单元不饱和脂肪酸形成超O3化物。

Compared with diolefine rubber,EPDM has less double bond.

与二烯烃橡胶相比,EPDM的双键很少。

Ring closing metathesis (RCM) of dienes to cycloalkene provides an important tool for C-C double bond formation catalyzed by metal carbene.

关环转换反应是形成碳碳双键的重要反应之一,即双烯化合物在金属碳烯催化下关环得到环烯类化合物。

Ethyl phenylacrylate intermediate bringing a double bond was introduced first,which is subsequently transformed into triketone and then DCM was obtained with high purity.

采用具有烯烃架的β-苯基丙烯酸酯为中间体先引入双键,再经过三酮合环制备乙烯基吡喃。

Results indicate interestingly that the double bond of GMA polymerized with polystyryl carbanion and the molar ratio of epoxy end group and polystyrene oligomer can be adjusted.

在GMA与聚苯乙烯阴离子反应的过程中，GMA在活性种的终端发生了聚合，所得产物中环氧端基与聚合产物的摩尔比可根据需要进。

Interestingly, in spite of its instability, the O3 molecule can be stabilized as an ozonide between the double bonds of a monounsaturated fatty acid such as oleic acid.

有趣的是，尽管不稳定，超氧O3分子却能以双键结合安定于像油酸那样的单元不饱和脂肪酸形成超氧O3化物。

Compared with diolefine rubber,EPDM has less double bond.

二烯烃橡胶相比,EPDM的双键很少。

Ring closing metathesis (RCM) of dienes to cycloalkene provides an important tool for C-C double bond formation catalyzed by metal carbene.

关环转换反应是形成碳碳双键的重要反应之一,即双烯化合物在金属碳烯催化下关环得到环烯类化合物。

Ethyl phenylacrylate intermediate bringing a double bond was introduced first,which is subsequently transformed into triketone and then DCM was obtained with high purity.

采用具有烯烃架的β-苯丙烯酸酯为中间体先引入双键,再经过三酮合环制备乙烯吡喃。

Results indicate interestingly that the double bond of GMA polymerized with polystyryl carbanion and the molar ratio of epoxy end group and polystyrene oligomer can be adjusted.

在GMA聚苯乙烯阴离子反应的过程中，GMA在活性种的终发生了聚合，所得产物中环氧聚合产物的摩尔比可根据需要进行调节。

Interestingly, in spite of its instability, the O3 molecule can be stabilized as an ozonide between the double bonds of a monounsaturated fatty acid such as oleic acid.

有趣的是，尽管不稳定，超氧O3分子却能以双键结合安定于像油酸那样的单元不饱和脂肪酸形成超氧O3化物。

Compared with diolefine rubber,EPDM has less double bond.

与二烯烃橡胶相比,EPDM的双键很少。

Ring closing metathesis (RCM) of dienes to cycloalkene provides an important tool for C-C double bond formation catalyzed by metal carbene.

关环转换反应是形成碳碳双键的重要反应之一,即双烯化合物在金属碳烯催化下关环得到环烯类化合物。

Ethyl phenylacrylate intermediate bringing a double bond was introduced first,which is subsequently transformed into triketone and then DCM was obtained with high purity.

采用具有烯烃架的β-苯基丙烯酸酯为中间体先引入双键,再经过三酮合环制备乙烯基吡喃。

Results indicate interestingly that the double bond of GMA polymerized with polystyryl carbanion and the molar ratio of epoxy end group and polystyrene oligomer can be adjusted.

在GMA与聚苯乙烯阴离子反应的过程中，GMA在活性种的终端发生了聚合，所得产物中环氧端基与聚合产物的摩尔比可根据需要进行调。

Interestingly, in spite of its instability, the O3 molecule can be stabilized as an ozonide between the double bonds of a monounsaturated fatty acid such as oleic acid.

有的是，尽管不稳定，超氧O3分子却能以双键结合安定于像油酸那样的单元不饱和脂肪酸形成超氧O3化物。

Compared with diolefine rubber,EPDM has less double bond.

与二烯烃橡胶相比,EPDM的双键很少。

Ring closing metathesis (RCM) of dienes to cycloalkene provides an important tool for C-C double bond formation catalyzed by metal carbene.

关环转换反应是形成碳碳双键的重要反应之一,即双烯在金属碳烯催下关环得到环烯类。

Ethyl phenylacrylate intermediate bringing a double bond was introduced first,which is subsequently transformed into triketone and then DCM was obtained with high purity.

采用具有烯烃架的β-苯基丙烯酸酯为中间体先引入双键,再经过三酮环烯基吡喃。

Results indicate interestingly that the double bond of GMA polymerized with polystyryl carbanion and the molar ratio of epoxy end group and polystyrene oligomer can be adjusted.

在GMA与聚苯烯阴离子反应的过程中，GMA在活性种的终端发生了聚，所得产中环氧端基与聚产的摩尔比可根据需要进行调节。

Interestingly, in spite of its instability, the O3 molecule can be stabilized as an ozonide between the double bonds of a monounsaturated fatty acid such as oleic acid.

有趣的是，尽管不稳定，超氧O3分子却能以双键结安定于像油酸那样的单元不饱和脂肪酸形成超氧O3。

Compared with diolefine rubber,EPDM has less double bond.

烃橡胶相比,EPDM的双键很少。

Ring closing metathesis (RCM) of dienes to cycloalkene provides an important tool for C-C double bond formation catalyzed by metal carbene.

关环转换反应是形成碳碳双键的重要反应之一,即双化合在金属碳催化下关环得到环类化合。

Ethyl phenylacrylate intermediate bringing a double bond was introduced first,which is subsequently transformed into triketone and then DCM was obtained with high purity.

采用具有烃架的β-苯基丙酸酯为间体先引入双键,再经过三酮合环制备乙基吡喃。

Results indicate interestingly that the double bond of GMA polymerized with polystyryl carbanion and the molar ratio of epoxy end group and polystyrene oligomer can be adjusted.

在GMA聚苯乙阴离子反应的过程，GMA在活性种的终端发生了聚合，所得环氧端基聚合的摩尔比可根据需要进行调节。

Interestingly, in spite of its instability, the O3 molecule can be stabilized as an ozonide between the double bonds of a monounsaturated fatty acid such as oleic acid.

有趣的是，尽管不稳定，超氧O3分子却能以双键结合安定于像油酸那样的单元不饱和脂肪酸形成超氧O3化。

Compared with diolefine rubber,EPDM has less double bond.

二烯烃橡胶相比,EPDM的双键很少。

Ring closing metathesis (RCM) of dienes to cycloalkene provides an important tool for C-C double bond formation catalyzed by metal carbene.

关环转换反应是形成碳碳双键的重要反应之一,即双烯化合物在金属碳烯催化下关环得到环烯类化合物。

Ethyl phenylacrylate intermediate bringing a double bond was introduced first,which is subsequently transformed into triketone and then DCM was obtained with high purity.

采用具有烯烃架的β-苯丙烯酸酯为中间体先引入双键,再经过三酮合环制备乙烯吡喃。

Results indicate interestingly that the double bond of GMA polymerized with polystyryl carbanion and the molar ratio of epoxy end group and polystyrene oligomer can be adjusted.

在GMA苯乙烯阴离子反应的过程中，GMA在活性种的终端发生了合，所得产物中环氧端合产物的摩尔比可根据需要进行调节。

Interestingly, in spite of its instability, the O3 molecule can be stabilized as an ozonide between the double bonds of a monounsaturated fatty acid such as oleic acid.

有趣的是，尽管不稳定，超氧O3分子却能以双键结合安定于像油酸那样的单元不饱和脂肪酸形成超氧O3化物。

Compared with diolefine rubber,EPDM has less double bond.

与二烯烃橡胶相比,EPDM的很少。

Ring closing metathesis (RCM) of dienes to cycloalkene provides an important tool for C-C double bond formation catalyzed by metal carbene.

关环转换反应是形成碳碳的重要反应之一,即烯化合物在金属碳烯催化下关环得到环烯类化合物。

Ethyl phenylacrylate intermediate bringing a double bond was introduced first,which is subsequently transformed into triketone and then DCM was obtained with high purity.

采用具有烯烃架的β-苯基丙烯酸酯为中间体先引入,再经过三酮合环制备乙烯基吡喃。

Results indicate interestingly that the double bond of GMA polymerized with polystyryl carbanion and the molar ratio of epoxy end group and polystyrene oligomer can be adjusted.

在GMA与聚苯乙烯阴离子反应的过程中，GMA在活性种的终端发生了聚合，所得产物中环氧端基与聚合产物的摩尔比可要进行调节。

Interestingly, in spite of its instability, the O3 molecule can be stabilized as an ozonide between the double bonds of a monounsaturated fatty acid such as oleic acid.

有趣的是，尽管不稳定，超氧O3分子却能以结合安定于像油酸那样的单元不饱和脂肪酸形成超氧O3化物。