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Ring-Opening Polymerization of THF by Aryloxo-Modified (Imido)vanadium(V)-alkyl Complexes and Ring-Opening Metathesis Polymerization by Highly Active V(CHSiMe3)(NAd)(OC6F5)(PMe3)2

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Figshare2016-02-20 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Ring_Opening_Polymerization_of_THF_by_Aryloxo_Modified_Imido_vanadium_V_alkyl_Complexes_and_Ring_Opening_Metathesis_Polymerization_by_Highly_Active_V_CHSiMe_sub_3_sub_NAd_OC_sub_6_sub_F_sub_5_sub_PMe_sub_3_sub_sub_2_sub_/2503042
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Ring-opening polymerizations of THF using V­(NR)­(CH2SiMe3)­(OAr)2 [R = 2,6-Me2C6H3, 1-adamantyl (Ad), Ph; Ar = 2,6-Me2C6H3, C6F5] proceeded in a living manner in the presence of [Ph3C]­[B­(C6F5)4], affording high molecular weight polymers with low PDI (Mw/Mn) values: the observed activity (initiation efficiency) was affected by the arylimido and aryloxo ligands employed. A new vanadium­(V)-alkylidene, V­(CHSiMe3)­(NAd)­(OC6F5)­(PMe3)2, prepared from V­(NAd)­(CH2SiMe3)2(OC6F5) by α-hydrogen elimination in n-hexane in the presence of PMe3 at 25 °C, exhibited remarkable catalytic activity for ring-opening metathesis polymerization of norbornene: the activity at 25 °C was higher than those by the reported vanadium­(V)-alkylidenes and ordinary Mo­(CHCMe2Ph)­(N-2,6-iPr2-C6H3)­(OtBu)2.
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2016-02-20
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