首页> 外文期刊>Journal of the American Chemical Society >SYNTHESIS AND APPLICATIONS OF RUCL2(=CHR')(PR(3))(2) - THE INFLUENCE OF THE ALKYLIDENE MOIETY ON METATHESIS ACTIVITY
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SYNTHESIS AND APPLICATIONS OF RUCL2(=CHR')(PR(3))(2) - THE INFLUENCE OF THE ALKYLIDENE MOIETY ON METATHESIS ACTIVITY

机译:RUCL2(= CHR')(PR(3))(2)的合成及应用-炔基部分对复分解活性的影响

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The reactions of RuCl2(PPh(3))(3) with a number of diazoalkanes were surveyed, and alkylidene transfer to give RuCl2(=CHR)(PPh(3))2 (R = Me (1), Et (2)) and RuCl2(=CH-p-C(6)H(4)X)(PPh(3))(2) (X = H (3), NMe(2) (4), OMe (5), Me (6), F (7), Cl (8), NO2 (9)) was observed for alkyl diazoalkanes RCHN(2) and various para-substituted aryl diazoalkanes p-C(6)H(4)XCHN(2). Kinetic studies on the living ring-opening metathesis polymerization (ROMP) of norbornene using complexes 3-9 as catalysts have shown that initiation is in all cases faster than propagation (k(i)/k(p) = 9 for 3) and that the electronic effect of X on the metathesis activity of 3-9 is relatively small. Phosphine exchange in 3-9 with tricyclohexylphosphine leads to RuCl2(=CH-p-C(6)H(4)X)(PCy(3))(2) 10-16, which are efficient catalysts for ROMP of cyclooctene (PDI = 1.51-1.63) and 1,5-cyclooctadiene (PDI = 1.56-1.67). The crystal structure of RuCl2(=CH-p-C6H4Cl)(PCy(3))(2) (15) indicated a distorted square-pyramidal geometry, in which the two phosphines are trans to each other, and the alkylidene unit lies in the Cl-Ru-Cl plane. The benzylidenes RuCl2(=CHPh)(PR(3))(2) (R = Cy (cyclohexyl) (10), Cp (cyclopentyl) (17), i-Pr (18)) are quantitatively available via one-pot synthesis with RuCl2(PPh(3))(3), PhCHN(2), and PR(3) as reaction components. 10 is an efficient catalyst for metathesis of acyclic olefins: On reaction with excess ethylene, the methylidene complex RuCl2(=CH2)(PCy(3))(2) (19) is formed quantitatively and various alkylidene compounds RuCl2(=CHR)(PCy(3))(3) (R = Me (20), Et (21), n-Bu (22)) are isolated as the kinetic products from the reaction of 10 with an excess of the corresponding terminal or disubstituted olefins. Metathesis of conjugated and cumulated olefins with 10 results in the formation of vinylalkylidene and vinylidene complexes, as shown by the synthesis of RuCl2(=CHCH=CH2)(PCy(3))(2) (23) and RuCl2(=C=CH2)(PCy(3))(2) (24) from 1,3-butadiene or 1,2-propadiene, respectively. Also, functional groups such as -OAc, -Cl, and -OH can be introduced into the alkylidene moiety via cross metathesis with the appropriate alkene.
机译:考察了RuCl2(PPh(3))(3)与许多重氮烷的反应,并进行了亚烷基转移,得到RuCl2(= CHR)(PPh(3))2(R = Me(1),Et(2) )和RuCl2(= CH-pC(6)H(4)X)(PPh(3))(2)(X = H(3),NMe(2)(4),OMe(5),Me(6 ),对于烷基重氮烷烃RCHN(2)和各种对位取代的芳基重氮烷烃pC(6)H(4)XCHN(2),观察到F(7),Cl(8),NO2(9))。使用配合物3-9作为催化剂对降冰片烯的活性开环易位聚合(ROMP)进行动力学研究表明,在所有情况下,引发的速度都快于扩散(3的k(i)/ k(p)= 9),并且X对3-9的复分解活性的电子影响相对较小。与三环己基膦在3-9中进行膦交换可生成RuCl2(= CH-pC(6)H(4)X)(PCy(3))(2)10-16,这是有效的环辛烯ROMP催化剂(PDI = 1.51 -1.63)和1,5-环辛二烯(PDI = 1.56-1.67)。 RuCl2(= CH-p-C6H4Cl)(PCy(3))(2)(15)的晶体结构显示了扭曲的方锥几何形状,其中两个膦彼此间互反,亚烷基单元位于Cl-Ru-Cl平面。亚苄基RuCl2(= CHPh)(PR(3))(2)(R = Cy(环己基)(10),Cp(环戊基)(17),i-Pr(18))可通过一锅合成法定量获得以RuCl2(PPh(3))(3),PhCHN(2)和PR(3)作为反应成分。 10是用于无环烯烃复分解的有效催化剂:与过量的乙烯反应后,定量形成亚甲基络合物RuCl2(= CH2)(PCy(3))(2)(19)和各种亚烷基化合物RuCl2(= CHR)( PCy(3))(3)(R = Me(20),Et(21),n-Bu(22))作为动力学产物从10与过量的相应末端或二取代烯烃的反应中分离出来。 RuCl2(= CHCH = CH2)(PCy(3))(2)(23)和RuCl2(= C = CH2)的合成表明,共轭烯烃和累积烯烃与10的复分解导致乙烯基亚烷基和亚乙烯基络合物的形成。 )(PCy(3))(2)(24)分别来自1,3-丁二烯或1,2-丙二烯。同样,可以通过与合适的烯烃的交叉复分解将诸如-OAc,-Cl和-OH之类的官能团引入亚烷基部分。

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