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.

转换反应是形成碳碳键的重要反应之一,即烯化合物在金属碳烯催化下到烯类化合物。

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在活性种的终端发生了聚合，所产物中氧端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，超氧O3分子却能以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.

与二烃橡胶相比,EPDM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反应之一,即双化合物在金属碳催化下关环得到环类化合物。

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

采用具有烃架β-基丙酸酯为中间体先引入双键,再经过三酮合环制备基吡喃。

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与聚阴离子反应过程中，GMA在活性种终端发生了聚合，所得产物中环氧端基与聚合产物摩尔比可根据需进行调节。

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.

关环转换形成碳碳双键的重要之一,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-苯基丙烯酸酯为间体先引入双键,再经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与聚苯乙烯阴离子的，GMA在活性种的终端发生了聚合，所得产物环氧端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，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重要反应之一,即双烯化合在金属碳烯催化下关环得到环烯类化合。

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过程中，GMA在活性种终端发生了聚合，所得中环氧端基与聚合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双键的重要反应之一,即双化合物在金催化下关环得到环类化合物。

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

采用具有烃架的β-苯基丙酸酯为中间体先引入双键,再经合环制备乙基吡喃。

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与聚苯乙阴离子反应的程中，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.

与二橡胶相比,EPDM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重要反应之一,即双化合物在金属碳催化下关环得到环类化合物。

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β-苯基丙酸酯为中间体先引入双键,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与聚苯乙阴离子反应过程中，GMA在活性种终端发生了聚合，所得产物中环氧端基与聚合产物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,即双化合物在金属碳催化下关得到化合物。

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

采用具有烃架的β-苯基丙酸酯为先引入双键,再经过三酮合制备乙基吡喃。

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与聚苯乙阴离子反应的过程，GMA在活性种的终端发生了聚合，所得产物氧端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.

具有烃架的β-苯基酯为中间体先引入双键,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与聚苯乙阴离子反应的过程中，GMA在活性种的终端发生了聚合，所得产中环氧端基与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那样的单元不饱和脂肪形成超氧O3化。