Visible light-mediated gold-catalysed carbon(sp2)–carbon(sp) cross-coupling† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c5sc03025k

A new method for the alkynylation of aryldiazonium salts with TMS-alkynes via dual gold and photoredox catalysis is described.


Introduction
For over a decade, homogeneous gold catalysis has been investigated because it provides access to novel modes of reactivity and enables rapid generation of complex molecular architectures. 1 However, in contrast to other low-valent late transition metal catalysts, the majority of gold(I) complexes are unreactive towards the oxidative addition of aryl and vinyl halides and pseudohalides. 2 Consequently, most gold-catalysed cross-coupling reactions have required sacricial oxidants to access the +3 oxidation state. 3 For example, this reactivity platform has been exploited in a gold-catalysed oxidative coupling of organosilanes and 1,2-alkene functionalizations (Scheme 1A). As an alternative, visible light-mediated oxidative addition of aryldiazoniums has emerged as a method for the generation of the requisite gold(III) intermediates via photoredox catalysis, thereby obviating the need for sacricial oxidants. 4 These gold(III) intermediates have been intercepted by a variety of nucleophiles in dual catalytic photoredox-gold reactions (Scheme 1B).
Although aryldiazoniums and photoredox catalysts provide an efficient method to generate gold(III) intermediates, several challenges must be addressed in order to facilitate carboncarbon cross-coupling via these species. First, aryldiazonium salts are highly electrophilic and reactive towards many classes of nucleophilic coupling partners. Aryldiazoniums are generally decomposed under Kumada and Negishi coupling conditions and do not tolerate ligand additives and stoichiometric bases employed in the majority of Suzuki, Sonogashira and Hiyama coupling reactions. 5 Second, as visible light-mediated oxidative addition of aryldiazoniums is proposed to proceed through radical intermediates, nucleophilic coupling partners that can participate in single electron transfer, such as organotin and organotriuoroborates compounds, are problematic. 6 Inspired by the oxidative coupling of organosilanes, we envisioned that the gold(III) complexes generated via photoredox catalysis might undergo transmetalation with organosilanes, generating an intermediate poised for carbon-carbon bond formation through reductive elimination. 7,8 Results and discussions While aryldiazonium tetrauoroborates have been shown to react with halo-, azido-, allyl-and thiotrimethylsilanes, their reactions with alkynyltrimethylsilanes has not been previously reported. 9 Additionally, previous reports of organosilane transmetallation with gold lead us to hypothesize that the transmetallation of alkynyltrimethylsilanes to gold(III) intermediates might result in productive cross-coupling. On the basis of this hypothesis, we examined the combined gold/photoredox coupling of 1 equivalent of aryldiazonium salt 1a and 1 equivalent of alkynyltrimethylsilane 2.
Evaluation of reaction conditions showed that the combination of Ar 3 PAuCl and Ru(bpy) 3 (PF 6 ) 2 , in acetonitrile gave the highest yield of aryl alkyne 3a (Table 1). Changing either the solvent or the photoredox catalyst proved detrimental to the yield of the desired product. With respect to the ligands on the gold catalyst, both electronic and steric factors impacted the efficiency of the cross-coupling. For example, electron-decient triarylphosphine ligands resulted in signicantly lower yield of 3a (Table 1, entry 10). The sterics of the ligand showed an even more dramatic effect on reaction yield. The reaction conducted with (p-tol) 3 PAuCl provided 72% yield of the desired product, while the much more hindered (o-tol) 3 PAuCl-catalysed reaction only provided 17% yield of 3a (Table 1, entry 11 and 12). The yield of product was lower when tricyclohexylphosphinegold(I) chloride was used as catalyst instead of triphenylphoshinegold(I) chloride (Table 1, entry 13). Gold(I) complexes of dialkylbiarylphosphine were also examined, but all showed less than 5% yield due to the combined effect of dialkyl groups and the steric effect of biaryl groups. Finally, no coupling product was observed in the absence of the ruthenium catalyst (entry 14) or when the reaction was conducted in the dark (entry 15).
With an optimized catalyst system in hand, the scope with respect to the aryldiazonium coupling partner was examined ( Table 2). The yields of alkynylation reactions of electron-poor aryldiazonium salts were generally higher than those of reactions with electron-rich aryldiazonium coupling partners. It should be noted that the intrinsic instability of orthosubstituted aryldiazonium salts limited their use in this transformation (Table 2, entry 3k and 3l). It is also noteworthy that all halogen substitutions on the aryldiazonium coupling partner were preserved during the coupling reaction. Bromo-and iodoaryldiazonium salts were readily coupled and leaving halides intact for use in further reactions (Table 2, 3b and 3j); this chemoselectivity is challenging under typical palladiumcatalysed Sonogashira coupling reactions. 10 The difference in reactivity of electron-rich and -poor aryldiazoniums may be the result of competing reaction pathways. Oxidative addition is believed to proceed through single electron reduction of aryldiazoniums and this process is preferred with electron-poor aryldiazonium salts. 4 On the other hand, the generation of aryl cations, through loss of dinitrogen, is facile with electron-rich aryldiazoniums. Correspondingly, we observed trace amount of desired product when benzenediazonium tetrauoroborate was heated at 60 C for 9 hours in the presence of 1-trimethylsilyl-2-(4-methoxy)phenylacetylene; however the same reactivity was not observed with 4-uorophenyldiazonium salts on the same conditions. The scope of alkynyltrimethylsilanes was also investigated ( Table 3). Both aryl-and alkylethynyltrimethylsilanes were coupled with modest to high product yields. o-Isopropylphenyl, biphenylyl and naphthylalkynyltrimethylsilanes participated in the gold-catalysed coupling (Table 3, 3m, 3n and 3o). Potentially sensitive benzylic and propargylic C-H and C-X bonds were well tolerated under the reaction conditions (Table 3, 3q, 3aa and 3s-v). Additionally, alkynyltrimethylsilane 3w was prepared in 78% yield from the coupling of aryldiazonium salt 1d and bis(trimethylsilyl) acetylene, providing a compliment to using trimethylsilylacetylene in a traditional Sonogashira coupling (Table 3, 3w).
coupled with 1d to generate terminal alkyne 3x, the yield was 15% with none of the corresponding silylacetylene 3w (Table 3). This observation suggests that, under the current base free reaction conditions, the silyl group plays a critical role in the coupling. To investigate this role, a set of reactions was performed by varying counteranions of aryldiazonium salts and silyl group identities of alkynylsilanes. The yield of coupling product was diminished as the steric hindrance of silyl group was increased ( Table 4, entry 1 and entries 4-7). While both tetrauoroborate and tosylate diazonium salts proved efficient coupling partners, the yield was diminished when hexa-uorophosphate salts were used. 11 Moreover, when the corresponding terminal alkyne was used instead of alkynyltrimethylsilanes, only 3% of the coupling product was observed ( Table 4, entry 8). 12 Taken together, these results suggests that transmetallation from the organosilane is critical for high efficiency of the current coupling reaction.
Other organotrimethylsilanes were tested under the optimized reaction conditions. While the reactions of aryl and vinylsilanes were complicated by competing reactions, 13,14 the gold/photoredox-catalysed coupling of allenyltrimethylsilane 4 provided propargylic compound 5 as the sole coupling product (Scheme 2). The product from aryl-allenyl reductive elimination and the other aryl-propargylic coupling isomer were prepared independently (Scheme 2, 6 and 7). We examined whether 6 was an intermediate that underwent isomerization to 5 facilitated by visible light and the photoredox catalyst. However, no isomerization was observed of 6 to either 5 or 7 under the reaction conditions. Therefore, the formation of 5 is best rationalized by transmetalation of 4 to the gold(III) intermediate, followed by 1,3-migration and aryl-propargyl reductive elimination.