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首页> 外文期刊>Organometallics >Molybdenum and Tungsten Alkylidene and Metallacyclobutane Complexes That Contain a Dianionic Biphenolate Pincer Ligand
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Molybdenum and Tungsten Alkylidene and Metallacyclobutane Complexes That Contain a Dianionic Biphenolate Pincer Ligand

机译:包含双阴离子双酚盐夹配体的钼和钨亚烷基和金属环丁烷配合物

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摘要

Molybdenum imido alkylidene and tungsten oxo alkylidene complexes that contain a tridentate "pincer" [ONO](2-) ligand have been prepared and treated with ethylene to give unsubstituted metallacyclobutane complexes that have a 16e count. Both Mo and W metallacyclobutane complexes exchange C2D4 into the metallacyclobutane ring at 22 degrees C at a rate that is first order in metal and zero order in C2D4. These metallacycles lose ethylene at least 10(4)-10(5) times slower than reported 14e unsubstituted Mo and W metallacyclobutane complexes that have been explored in the literature that have a TBP geometry with the metallacyclobutane ring bound in the equatorial positions. Our studies suggest that breaking up the metallacyclobutane ring in these 16e d(0) Mo or W complexes is slow because a 14e TBP metallacyclobutane complex cannot be accessed readily.
机译:已经制备了含有三齿“钳” [ONO](2-)配体的亚氨基钼亚烷基亚烷基和氧代亚烷基钨亚烷基配合物,并用乙烯处理,得到具有16e数的未取代的金属环环丁烷配合物。 Mo和W金属环丁烷络合物都在22摄氏度下以金属中的第一级和C2D4中的零级的速率将C2D4交换到金属环丁烷环中。这些金属环化合物损失的乙烯至少比报道的14e未取代的Mo和W金属环环丁烷络合物慢至少10(4)-10(5)倍,该文献已在文献中进行了研究,这些配合物具有TBP几何结构,金属环环丁烷环键合在赤道位置。我们的研究表明,在这些16e d(0)Mo或W配合物中分解金属环丁烷环的速度很慢,因为14e TBP金属环丁烷配合物不易获得。

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