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Synthetic and Structural Studies of [AuCl3(NHC)] Complexes
A series of N-heterocyclic carbene complexes [AuCl(NHC)] 1 [NHC: IPr, a; SIPr, b; IPrMe, c; IPrCl, d; IMes, e; SIMes, f; I t Bu, g; IAd, h; and ICy, i] were reacted with chlorine gas or PhICl2 to afford [AuCl3(IPr)], 2a; [AuCl3(SIPr)], 2b; [AuCl3(IPrMe)], 2c; [AuCl3(IPrCl)], 2d; [AuCl3(IMes)], 2e; [...
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Published in: | Organometallics 2010-01, Vol.29 (2), p.394-402 |
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creator | Gaillard, Sylvain Slawin, Alexandra M. Z Bonura, Allen T Stevens, Edwin D Nolan, Steven P |
description | A series of N-heterocyclic carbene complexes [AuCl(NHC)] 1 [NHC: IPr, a; SIPr, b; IPrMe, c; IPrCl, d; IMes, e; SIMes, f; I t Bu, g; IAd, h; and ICy, i] were reacted with chlorine gas or PhICl2 to afford [AuCl3(IPr)], 2a; [AuCl3(SIPr)], 2b; [AuCl3(IPrMe)], 2c; [AuCl3(IPrCl)], 2d; [AuCl3(IMes)], 2e; [AuCl3(SIMes)], 2f; [AuCl3(I t Bu)], 2g; [AuCl3(IAd)], 2h; and [AuCl3(ICy)], 2i, respectively. Complete characterization by 1H and 13C NMR spectroscopies as well as by single-crystal X-ray diffraction was performed in order to discern electronic and structural differences between organogold(I/III) congeners. Calculations of the buried volume of the NHC ligand in complexes [AuCl3(NHC)] 2 were also performed in order to evaluate the steric hindrance of the NHC. These data permit comparisons with the related complexes [AuCl(NHC)] 1 and [AuBr3(NHC)]. |
doi_str_mv | 10.1021/om900814e |
format | article |
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Z ; Bonura, Allen T ; Stevens, Edwin D ; Nolan, Steven P</creator><creatorcontrib>Gaillard, Sylvain ; Slawin, Alexandra M. Z ; Bonura, Allen T ; Stevens, Edwin D ; Nolan, Steven P</creatorcontrib><description>A series of N-heterocyclic carbene complexes [AuCl(NHC)] 1 [NHC: IPr, a; SIPr, b; IPrMe, c; IPrCl, d; IMes, e; SIMes, f; I t Bu, g; IAd, h; and ICy, i] were reacted with chlorine gas or PhICl2 to afford [AuCl3(IPr)], 2a; [AuCl3(SIPr)], 2b; [AuCl3(IPrMe)], 2c; [AuCl3(IPrCl)], 2d; [AuCl3(IMes)], 2e; [AuCl3(SIMes)], 2f; [AuCl3(I t Bu)], 2g; [AuCl3(IAd)], 2h; and [AuCl3(ICy)], 2i, respectively. Complete characterization by 1H and 13C NMR spectroscopies as well as by single-crystal X-ray diffraction was performed in order to discern electronic and structural differences between organogold(I/III) congeners. Calculations of the buried volume of the NHC ligand in complexes [AuCl3(NHC)] 2 were also performed in order to evaluate the steric hindrance of the NHC. 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Calculations of the buried volume of the NHC ligand in complexes [AuCl3(NHC)] 2 were also performed in order to evaluate the steric hindrance of the NHC. These data permit comparisons with the related complexes [AuCl(NHC)] 1 and [AuBr3(NHC)].</description><issn>0276-7333</issn><issn>1520-6041</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNptj8FKxDAURYMoWEcX_kE3grOovuQlTepuKOoIgy5GVyLl0STYoZ0OSQvO31sZceXq3sXhcg9jlxxuOAh-23cFgOHSHbGEKwFZDpIfswSEzjONiKfsLMYNAOQaRcLu1vvt8OmGpk5pa9P1EMZ6GAO1Ux1t42La-_R9MZYtXj8vy_lHWvbdrnVfLp6zE09tdBe_OWNvD_ev5TJbvTw-lYtVRkIVQ6Y0gQBpdG45aSlBknIF9xzJgDGCCC0pL41Fgzn6QllT54QStOOF9zhj88NuHfoYg_PVLjQdhX3FofqRrv6kJ_bqwFIdq00_hu307B_uG8j8U6w</recordid><startdate>20100125</startdate><enddate>20100125</enddate><creator>Gaillard, Sylvain</creator><creator>Slawin, Alexandra M. 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Complete characterization by 1H and 13C NMR spectroscopies as well as by single-crystal X-ray diffraction was performed in order to discern electronic and structural differences between organogold(I/III) congeners. Calculations of the buried volume of the NHC ligand in complexes [AuCl3(NHC)] 2 were also performed in order to evaluate the steric hindrance of the NHC. These data permit comparisons with the related complexes [AuCl(NHC)] 1 and [AuBr3(NHC)].</abstract><pub>American Chemical Society</pub><doi>10.1021/om900814e</doi><tpages>9</tpages></addata></record> |
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title | Synthetic and Structural Studies of [AuCl3(NHC)] Complexes |
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