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Laser Flash Photolysis Studies of Some Dimethylgermylene Precursors

机译:某些二甲基锗烯前体的激光闪光光解研究

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摘要

The laser flash photolysis of dodecamethylcyclohexagermane (1) and dimethylphenyl(trimethylsilyl)germane (5), two known photochemical precursors to dimethylgermylene (GeMe2), has been reinvestigated. Laser flash photolysis of I in hexane solution affords markedly different results than were reported in an earlier study of this compound in cyclohexane. The present study shows it to yield two primary transient products, one exhibiting lambda(max) = 490 nm and lifetime tau <= 10 ns and a second that exhibits lambda(max) = 470 nm and decays on the microsecond time scale with second-order kinetics, with the concomitant growth of absorptions centered at lambda(max) = 370 nm due to tetramethyldigermene (Ge2Me4). The spectrum and absolute rate constants for quenching of the 470 nm species by acetic acid, 2,3-dimethyl-1,3-butadiene (DMB), CCl4, and oxygen in hexane, as well as the transient behavior observed in the presence of millimolar concentrations of THF, are all quite similar to those established recently for GeMe2 using 1-germacyclopent-3-ene derivatives as precursors. Two different transient products dominate the time-resolved spectra obtained from laser flash photolysis of 5 under similar conditions, one exhibiting lambda(max) = 300 nm and tau approximate to 20 mu s and a second exhibiting lambda(max) = 430 nm and tau approximate to 4 mu s. The latter species was assigned to GeMe2 in earlier studies; it is re-assigned in the present work to the conjugated germene (6) derived from 1,3 trimethylsilyl migration into the ortho-position of the phenyl ring in 5, on the basis of comparisons of the spectrum and absolute rate constants for quenching of the species by oxygen, DMB, CCl4, acetic acid, and acetone to those reported previously for the homologous silene derivative (11) and the corresponding 1,1-diphenyl-substituted analogues of the germene (12) and the silene (13). Weak transient absorptions consistent with the postpulse formation of Ge2Me4 are also detectable from 5 in deoxygenated hexanes, but GeMe2 itself cannot be detected.
机译:十二甲基环六锗烷(1)和二甲基苯基(三甲基甲硅烷基)锗烷(5)(二甲基锗烷(GeMe2)的两种已知的光化学前体)的激光快速光解已被重新研究。 I在己烷溶液中的激光快速光解得到的结果与先前在环己烷中对该化合物的早期研究中报道的结果截然不同。本研究表明,它可产生两种主要的瞬态产物,一种表现出的lambda(max)= 490 nm,寿命tau <= 10 ns,另一种表现出的lambda(max)= 470 nm,并在微秒级上衰减,其次为由于四甲基二茂铁(Ge2Me4),吸收动力学同时出现在λ(max)= 370 nm处。乙酸,2,3-二甲基-1,3-丁二烯(DMB),CCl4和己烷中的氧气淬灭470 nm物质的光谱和绝对速率常数,以及在存在下的瞬态行为毫摩尔浓度的THF与使用1-germacyclopent-3-ene衍生物作为前体的GeMe2最近确定的浓度非常相似。在相似的条件下,两种不同的瞬态产物主导了5种激光闪光光解所获得的时间分辨光谱,其中一种表现出的lambda(max)= 300 nm,tau约为20μs,第二种表现出的lambda(max)= 430 nm和tau约4 s。在较早的研究中,后者被分配给了GeMe2。在光谱和绝对速率常数比较的基础上,在本工作中将其重新分配给由1,3三甲基甲硅烷基迁移到5中苯环邻位的共轭germ烯(6)。氧,DMB,CCl4,乙酸和丙酮的种类与先前报道的同种硅衍生物(11)以及相应的1,1-二苯基取代的种烯(12)和硅(13)类似。在脱氧己烷中,也可以从5中检测到与Ge2Me4的后脉冲形成相一致的弱瞬态吸收,但是GeMe2本身无法检测到。

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