作者:Oleg V. Gusev、Larisa N. Morozova、Tat'yana A. Peganova、Pavel V. Petrovskii、Nikolai A. Ustynyuk、Peter M. Maitlis
DOI:10.1016/0022-328x(94)80223-8
日期:1994.6
gave the exo-H isomer (1b, 25%) as well as the endo-H isomer (1a, 75%) of [Pt(η4-C5Me5H)Cl2]. The mixture reacted with AgBF4 in acetone at −78°C to give the mixed endo-H, exo-H isomeric dication solvate complexes [Pt(η4-C5Me5H)(acetone)x]2+(BF4−)2 (2a,b), which decompose at room temperature to give [Pt(η4-C5Me5H)(η5-C5Me5)]+BF4− (3). The same reaction of 1a,b in the presence of dienes (pentamethylcyclopentadiene
钾反应2氯铂酸4与五甲基环戊二烯,得到外-H异构体(1B,25%)以及所述内切-H异构体(1A [PT(η的,75%)4 -C 5我5 1H)氯2 ] 。将混合物用的AgBF反应4在丙酮在-78℃下,得到混合内-H,外切-H异构体二价阳离子溶剂化物配合物[铂(η 4 -C 5我5 H)(丙酮)X ] 2+(BF 4 −)2(图2a,b),其分解在室温下,得到[PT(η 4 -C 5我5 H)(η 5 -C 5我5)] + BF 4 - (3)。的相同的反应1A,b中的二烯(五甲基环戊二烯,环戊二烯,1,3-环己二烯,和1,5-环辛二烯)的存在下发生自发性的去质子化,得到单阳离子络合物,3,[PT(η 4 -C 5箱5 H)(η 5 -C 5箱5)] + BF 4 - (4A,b),[PT(η 4 -C 6 H ^ 8)(η 5 -C 5我5)] + BF 4 - (5),和[PT(η 4 -C