Ligand Substitution of RuII -Alkylidenes to Ru(bpy)3 2+ : Sequential Olefin Metathesis/Photoredox Catalysis.

Ruthenium(II) alkylidene complexes such as the Grubbs' 1st and 2nd generation catalysts undergo a ligand substitution with 2,2'-bipyridine, which readily leads to the common photoredox catalyst Ru(bpy)3 2+ . The application of this catalyst transformation in sequential olefin metathesis/photoredox catalysis is demonstrated by way of ring-closing metathesis (RCM)/photoredox ATRA reactions.

In sequential catalysis,1 which may also be referred to as “assisted tandem catalysis”,2 a single catalytically active metal center is utilized in two (or more) consecutive orthogonal catalytic reactions. Key to this sustainable approach to catalysis is a sufficiently mild ligand substitution of a given metal catalyst in the presence of a respective organic reaction intermediate, which by contrast to conventional multistep synthesis is not isolated between the individual steps, yet avoiding its labor‐intensive and waste‐generating purification (Scheme 1 a). In the context of sequential catalysis, ruthenium‐based catalysts, including RuII–alkylidenes,3 have received particular attention. Owing to their large number of stable oxidation states ranging from −2 to +8, ruthenium catalysts can mediate a plethora of synthetically highly useful organic transformations,4 and the particularly desired catalytic species are usually readily accessible by relatively simple chemical manipulations.

Scheme 1

a) Concept of sequential catalysis. b) and c) former and current contributions.

During the last decade, photoredox catalysis has emerged as a highly useful addition to the chemist's toolbox of synthetic methods, often enabling the synthesis of target structures which are difficult to access by classical approaches.5 However, hardly any examples of tandem or sequential catalytic protocols have been disclosed to date which encompass a photoredox reaction as key step. We demonstrated6 the successful sequential combination of a photoredox‐induced radical cationic Diels–Alder reaction7 with an oxidative 1,n‐diene cyclization.8 An in situ oxidation of the photoredox catalyst Ru(bpz)3 2+ to the strong oxidant RuVIII oxide allowed sequencing of the two orthogonal photochemical and thermal transformations in a one‐pot procedure, to eventually synthesize highly functionalized O‐heterocyclic products (Scheme 1 b).

Here, we report the reverse approach: we successfully sequenced a thermal reaction with a consecutive photoredox transformation. An olefin metathesis reaction9 was combined in one pot with a photocatalytic radical alkene 1,2‐difunctionalization;10 this new protocol was enabled by the in situ transformation of a RuII–alkylidene to Ru(bpy)3 2+ (Scheme 1 c).

We investigated the ligand substitution of Grubbs’ 1st and 2nd generation catalysts, G‐1 and G‐2, with 2,2′‐bipyridine (bpy) by UV/Vis monitoring (Scheme 2). For this purpose, dilute solutions of both RuII–alkylidenes were treated with larger excess of bpy in different solvents at elevated temperatures.

Scheme 2

Ligand substitution of Grubbs’ 1st and 2nd generation catalysts with 2,2′‐bipyridine (bpy) to photocatalyst Ru(bpy)3 2+. a) Time course of the reaction between catalyst G‐2 and bpy in the presence of AgBF4 analyzed by UV/Vis; c [Ru]=3.1×10−4  m in DCE. b) Time‐dependent development of the absorption at 455 nm for catalysts G‐1 and G‐2. DCE=Dichloroethane.

Upon reacting catalyst G‐1, we observed that the phosphines as well as the carbene ligand were rapidly displaced. However, the thermal reactions of G‐1 with bpy (10 up to 150 equiv with respect to RuII) in dichloroethane (DCE) at 80 °C, or even in dimethylformamide (DMF) at 140 °C in a sealed tube, would come to a halt at the relatively stable cis‐[Ru(bpy)2Cl2]11 (Figure S2). On the other hand, the desired global ligand substitutions of G‐1 and G‐2 could be achieved in the presence of silver(I) tetrafluoroborate (AgBF4) at 80 °C in DCE (Scheme 2 a and Figures S3, S4). In both cases, the characteristic absorption band of Ru(bpy)3 2+ at 455 nm evolved rapidly and G‐2 was almost fully converted after 30 min. In case of G‐1, the reaction required a longer period of 120–150 min and it also generated the blue oxo‐bridged dimer [(bpy)2(Cl)RuORu(Cl)(bpy)2]2+ as a byproduct, which we identified by its absorption spectrum12 and which was probably formed by hydrolysis of cis‐[Ru(bpy)2Cl2] with trace amounts of H2O, followed by AgI‐mediated oxidative dimerization13 (Figure S3). Despite the presence of this side product after the ligand substitution on catalyst G‐1, the resulting solutions were photochemically active as we could subsequently demonstrate.

The transformation of Grubbs’ 1st generation catalyst (G‐1) to Ru(bpy)3 2+ was successfully utilized in tandem olefin metathesis/photoredox reactions. As shown in Table 1, ortho‐allylstyrenes and further 1,n‐dienes 1 14 were converted to the indenes and cyclic alkenes 2 by ring‐closing metathesis (RCM) in DCE. Subsequent addition of 2,2′‐bipyridine (in a reduced excess of 10 equiv with respect to G‐1) and AgBF4 (2.5 equiv relative to G‐1) and heating to 80 °C for 3 h induced the ligand substitution of the RuII–alkylidene in the presence of the organic intermediate 2. The resulting reaction mixtures were concentrated to dryness, where after tosyl chloride (TsCl, 1.0 equiv) was added, and acetone as the optimal solvent for the adjacent photoredox step. Irradiation of the homogeneous solutions with blue LED light resulted in the clean chlorosulfonylation of the intermediary alkenes 2 by way of a redox neutral ATRA reaction15b, 16 of the sulfonyl halide with the alkene. While the presence of silver(I) salts showed no inhibitory effect on the photoredox‐induced reaction, the exchange of solvent was found necessary due to the limited solubility of the catalyst Ru(bpy)3(BF4)2 in DCE. When the sequence was carried out in DCE alone, product 3 a was formed in just 26 % compared to 57 % overall yield using acetone. trans‐configured products 3 were obtained exclusively in all cases, with the exception of the tetrahydrobenzo[7]annulene 3 i which was formed as a 5:1 mixture of diastereomers. Overall, the sequential protocol generated the 2‐chlorosulfones 3 in moderate to good isolated yields of up to 69 %, while one C−C and two C−het bonds were consecutively installed. The overall yields are well‐correlated with the combined isolated yields of the two individual steps, which were determined in independent experiments after chromatographic purification (see Supporting Information).

Table 1

One‐pot sequential RCM/photoredox chlorosulfonylation reactions.

#	1,n‐diene	RCM product	Step 1 yield [%]	Photoredox product	Step 2 yield [%]	Combined yield S1×S2 [%]	Sequential yield [%]
1			86		80	69	57
2			96		82	79	68
3			97		38	37	36
4			85		69	59	41
5			88		52	46	51
6			80		80	64	69
7			70		57	40	56
8			83		31	26	32
9			65		63	41	18

Experiments were conducted on 0.20 mmol scale. Sequential reactions: Step 1: diene 1 (0.20 mmol), 5 mol % G‐1 (10 μmol), DCE, R.T., 17 h, then bpy (0.10 mmol) and AgBF4 (25 μmol), 80 °C, 3 h. Step 2: TsCl (0.20 mmol), hv 460 nm LED, acetone, R.T., 48 h. Yields refer to isolated yields after chromatography.

#

In summary, we demonstrated for the first time the combination of olefin metathesis with photoredox catalysis in sequential one‐pot protocols, enabled by the in situ ligand substitution of RuII–alkylidenes to ruthenium(II)‐tris(bipyridine). The 2‐chlorosulfone products 3 were conveniently prepared by way of exemplary tandem RCM/photoredox ATRA reactions in moderate to good overall yields. Further applications of this concept are currently under investigation.

Conflict of interest

The authors declare no conflict of interest.

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Supplementary

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