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铑膦配合物的加压原位核磁氢谱研究 被引量:1
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作者 夏春谷 李达刚 +2 位作者 杨薇曼 孙衍文 杨天香 《化学学报》 SCIE CAS CSCD 北大核心 1990年第9期890-893,共4页
在近似工业反应条件下(H_2/CO=1∶1,1.0MPa,70℃),应用加温加压原位核磁共振技术,考察了铑膦配合物催化剂HRh(CO)(PPh_3)_3-PPh_3体系的烯烃醛化反应。结果表明,在烯烃醛化反应条件下,反应液中存在羰基氢化铑中间配合物,并在~1H NMR获... 在近似工业反应条件下(H_2/CO=1∶1,1.0MPa,70℃),应用加温加压原位核磁共振技术,考察了铑膦配合物催化剂HRh(CO)(PPh_3)_3-PPh_3体系的烯烃醛化反应。结果表明,在烯烃醛化反应条件下,反应液中存在羰基氢化铑中间配合物,并在~1H NMR获得了该配合物中Rh—H键的质子讯号。 展开更多
关键词 铑膦配合物 烯烃 醛化 氢谱 NMR
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烯烃氢甲酰化催化剂活性物种的原位~1H NMR研究 被引量:1
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作者 李达刚 夏春谷 +1 位作者 孙衍文 杨薇曼 《物理化学学报》 SCIE CAS CSCD 北大核心 1996年第1期71-74,共4页
The rhodium-phosphine complex catalyst Rh(CO)(acac)(PPh3)(Ⅰ) for 1-hexene hydroformylation was studied under the following reaction conditions: CO/H2=1(mole rate), pressure 1.0 MPa, temperature 25-120℃, by using the... The rhodium-phosphine complex catalyst Rh(CO)(acac)(PPh3)(Ⅰ) for 1-hexene hydroformylation was studied under the following reaction conditions: CO/H2=1(mole rate), pressure 1.0 MPa, temperature 25-120℃, by using the pres surized in-situ 1H NMR technique. Experimental results indicated that the formation of a rhodium hydride complex from (Ⅰ) began at room temperature and its amount increased with increasing of reaction temperature. This intermediate complex began to decompose at 100℃ and disapeared completely at 120℃ The intensity change of the proton signal was parallel to catalytical activity in hydroformylation of olefins. Under pure CO pressure the proton signal of Rh-H bond was not observed. There was a 0.2 ppm difference in proton chemical shifts of Rh-H bond under pure H2 pressure and under H2+CO pressure. The results showed that the rhodium-hydride carbonyl complex is the active intermediate in the industrial hydroformylation process. 展开更多
关键词 活性物种 NMR1 氢甲酰化 催化剂
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