2007
DOI: 10.1016/j.jorganchem.2006.09.044
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Synthesis and characterization of indenyl-functionalized N-heterocyclic carbene complex of Ni(II)

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Cited by 52 publications
(13 citation statements)
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“…In particular, the (533−534), [163] (535), [164] (536), [165] (543−544), [166] (545−546), [167] (548 [168]−557), [169] (558), [51] (559), [71] (560), [161] (561), [170] (562−563), [141] (565), [171] (566−567), [172] (568), [173] (569), [126d] (570−573), [174] (574), [175] (575−576), [176] (577), [177] (578), [178] (579), [106] (580−581), [179] (582−583), [151] (584−585), [180] (586−588), [181] (595−596), [182] (597−599), [183] (600−603), [184] (604), [185] (605−608), [186] (609), [185] (610−613), [187] (614−618), [188] (619−621), [189] (622−623), [185] (624−630), [190] (631), [191] (633−635), [192] (636), [193] (637), [194] (647) [195] and (648) [196] complexes were obtained by this pathway from the treatment of the free or the in situ generated NHC The third route is the oxidation method (Scheme 15) using which the (589−590), [197] (638) …”
Section: Neutral Chelated Ni(ii)−nhc Complexesmentioning
confidence: 99%
“…In particular, the (533−534), [163] (535), [164] (536), [165] (543−544), [166] (545−546), [167] (548 [168]−557), [169] (558), [51] (559), [71] (560), [161] (561), [170] (562−563), [141] (565), [171] (566−567), [172] (568), [173] (569), [126d] (570−573), [174] (574), [175] (575−576), [176] (577), [177] (578), [178] (579), [106] (580−581), [179] (582−583), [151] (584−585), [180] (586−588), [181] (595−596), [182] (597−599), [183] (600−603), [184] (604), [185] (605−608), [186] (609), [185] (610−613), [187] (614−618), [188] (619−621), [189] (622−623), [185] (624−630), [190] (631), [191] (633−635), [192] (636), [193] (637), [194] (647) [195] and (648) [196] complexes were obtained by this pathway from the treatment of the free or the in situ generated NHC The third route is the oxidation method (Scheme 15) using which the (589−590), [197] (638) …”
Section: Neutral Chelated Ni(ii)−nhc Complexesmentioning
confidence: 99%
“…Complexes of this type display catalytic activity in aryl dehalogenation and aryl amination, [3a] styrene polymerization in the presence of MAO, [2] and hydrothiolation of alkynes. [4] The related indenyl complexes [(η 3 -C 9 H 7 )-Ni(X)(NHC)] are moderately active in the oligomerization of ethylene [5] and styrene polymerization [6] in the presence of MAO or NaBPh 4 , respectively. Other NHC-supported Ni II complexes have also been tested for olefin polymerization [7] and carbon-carbon coupling reactions.…”
Section: Introductionmentioning
confidence: 99%
“…The same group also studied the polymerisation of styrene using a Ni II complex containing an NHC functionalised with a C3-bridged indenyl group, 74. [117] The indenyl group also appeared to improve the stability of the catalyst. …”
Section: A Number Of Examples Of Chelating Functionalised Nhc Complexmentioning
confidence: 99%