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作 者:刘诗咏[1] 周其忠[1] 金正能[1] 蒋华江[1] 姜玄珍[2]
机构地区:[1]台州学院医药化工学院,浙江临海317000 [2]浙江大学化学系,浙江杭州310027
出 处:《催化学报》2010年第5期557-561,共5页
基 金:Supported by the National Natural Science Foundation of China(20476092);the Foundation of Taizhou University(09ZD12)
摘 要:首次制备了十二烷基硫酸根(DS–)插层水滑石负载的纳米钯无膦配体型的Suzuki偶联反应催化剂.DS–进入到水滑石层间,使层间距从微孔增至2.9nm,从而有利于中等尺度的有机分子在催化剂表面的扩散.进一步以PdCl42–交换该水滑石得到DS–和PdCl42–双插层的水滑石.还原后可得到层间插有金属钯纳米团簇的水滑石.由于DS–插层后在水滑石层板间形成的空间有限,限制了Pd0团簇的进一步生长.作为一种亲油性的非均相催化剂,该类催化剂可有效促进卤代芳烃与苯硼酸的Suzuki偶联反应.催化剂循环使用5次后活性基本得以保持.The dodecylsulfate anion(DS-) embedded layered double hydroxide(LDH) supported nanopalladium catalyst(LDH-DS-Pd0) is a novel phosphine free recyclable heterogeneous catalytic system for palladium catalyzed Suzuki coupling reactions and has been prepared for the first time.The intercalation of DS-changed the interlayer spacing of LDH from a microsize to a mesosize(2.9 nm) range,which favors the diffusion of average sized organic molecules.The Pd0 clusters obtained from the reduction of PdCl42--interlayered LDH were intercalated between the LDH layers and hence the growth of Pd0 clusters was effectively hindered by the limited space created by the intercalation of DS-.This lipophilic catalyst was highly efficient in promoting the Suzuki reaction of aryl halides with phenylboronic acid.As a heterogeneous nanocatalyst,LDH-DS-Pd0 could be reused five times without significant loss of catalytic activity.
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