Abstract
Chlorinated compounds are ubiquitous. However, accumulation of chlorine-containing waste has a negative impact on human health and the environment due to the inapplicability of common disposal methods, such as landfill and incineration. Here we report a sustainable approach to valorize chlorine-containing hydrocarbon waste, including solids (chlorinated polymers) and liquids (chlorinated solvents), based on copper and palladium catalysts with a NaNO3 promoter. In the process, waste is oxidized to release the chlorine in the presence of N-directing arenes to afford valuable aryl chlorides, such as the FDA-approved drug vismodegib. The remaining hydrocarbon component is mineralized to afford CO, CO2 and H2O. Moreover, the CO and CO2 generated could be further utilized directly. Thus, chlorine-containing hydrocarbon waste, including mixed waste, can serve as chlorination reagents that neither generate hazardous by-products nor involve specialty chlorination reagents. This tandem catalytic approach represents a promising method for the viable management of a wide and diverse range of chlorine-containing hydrocarbon wastes.
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Main
Chlorinated compounds are ubiquitous in industrialized societies, as the physical and chemical properties of hydrocarbons are extensively modified (and improved) following chlorination. Thus, chlorine-containing hydrocarbons are widely used as plastics1,2, rubbers3,4,5, resins6,7 and solvents8,9,10, and have applications as intermediates used in the synthesis of agrochemicals and pharmaceuticals11,12, or are even present in agrochemical and pharmaceutical products13,14,15,16. Despite their enormous utility, chlorine-containing hydrocarbons are persistent in the environment or decompose to release toxic compounds, which can accumulate in the food chain. Exposure to chlorinated waste is even associated with suppression of the immune system and cancer, and yet methods to dispose of waste chlorine-containing hydrocarbons are currently inadequate17,18,19.
Chlorine-containing hydrocarbon waste is one of the most problematic types of waste because of the large scale of such waste and the common industrial approaches used to deal with it (landfill and incineration), which lead to the formation of hazardous products, including dioxins and corrosive gases such as HCl and Cl2. Safe disposal of chlorinated waste is therefore highly challenging (Fig. 1), with both pyrolysis and hydrocracking being unsuitable, as they result in the same problems as industrial incineration20,21,22,23,24. Although catalytic hydrocracking has been extensively investigated for upgrading a range of polymers, when applied to chlorinated polymers, deactivation of the catalyst is usually observed25,26,27,28. Hence, a two-step process consisting of dechlorination followed by decomposition has been reported, but this is expensive and largely unviable20,29,30,31,32,33. Recent approaches used for the destruction of polyvinyl chloride (PVC) are summarized in Supplementary Table 1 (note that HCl is produced in the majority of cases and is typically neutralized in a second step). Recently an electrochemical dechlorination method was reported for PVC, but only partial dechlorination (<20% conversion of Cl groups) was achieved and the method might be difficult to upscale34. Likewise, waste chlorinated solvents are problematic, with incineration being the conventional method used to dispose of them, as bioremediation is slow35,36. Electrochemical dechlorination of chlorinated hydrocarbon compounds has been reported, but suffers from low reaction rates and low Faradaic efficiencies (typically <50%)37,38. On account of these limitations for the reported treatments (which require corrosive reagents or lead to corrosive HCl emissions), there does not appear to be a sustainable, scalable method that efficiently eliminates different types of chlorinated hydrocarbon waste.
Extending on the achievements in Pd-catalysed C–H bond chlorination39,40,41,42 and Cu/NOx-catalysed C–C bond oxygenation43,44,45,46, we integrated the two reactions to afford a safe, sustainable and economically viable strategy to use chlorinated waste as chlorination reagents (Fig. 1). The approach simultaneously generates CO/CO2, via Cu/NOx-catalysed oxygenation of the hydrocarbon component, and chloride, which is transferred via Pd-catalysed C–H bond chlorination, to afford valuable aryl chlorides.
Results and discussion
Initial investigation of the reaction conditions
The high polarity of C–Cl bonds compared to C–H bonds in chlorine-containing hydrocarbon waste facilitates interactions with catalysts and can lead to their activation and functionalization47,48. Following C–Cl bond activation, transfer of the chlorine to a substrate, and mineralization of the hydrocarbon component of the waste, must be initiated. Commencing with conditions similar to those reported for the transfer of chlorine atoms in chlorophenol pollutants to arenes49, a Cu-catalysed aerobic reaction employing 7,8-benzoquinoline 1a as substrate and PVC (molecular weight, Mw: 100,000) as chlorination reagent, led to only trace quantities of the anticipated chlorinated product, namely, 10-chlorobenzoquinoline 1b (Supplementary Fig. 1). Since Pd catalysts are widely used to form C–X bonds42, bimetallic systems consisting of Cu and Pd catalysts were evaluated and found to generate the chlorinated product 1b (Fig. 2a, entries 1–5). The combination of homogeneous Cu(NO3)2 and heterogenous Pd catalysts (PdO, Pd/C, Pd(OH)2/C) remarkably enhances the yield of 1b to 83–85% (Fig. 2a, entries 1–3). Notably, the homogeneous Pd complexes are less efficient catalysts than heterogenous Pd catalysts (Fig. 2a, entries 4 and 5), which may be attributed to the strong coordination of the N-directing substrate leading to stable complexes that are less active50,51. Optimization of the NaNO3 concentration afforded the chlorinated product 1b in 99% yield (Fig. 2a, entry 7). The heterogenous PdO may be recovered by filtration and reused without loss in activity (Supplementary Fig. 11). Further details concerning the optimization of the reaction parameters are provided in Supplementary Figs. 1–10.
The gaseous products from the reaction were analysed by gas chromatography (GC) with CO and CO2 obtained in 15 and 81% yield, respectively, based on the carbon content of PVC (Fig. 2b), confirming that the hydrocarbon component of PVC is mineralized in near-quantitative yield (the formation of water was detected by 1H NMR spectroscopy; see below). Note that these gases were not observed in a control experiment without PVC. Notably, in the absence of PdO catalyst (Supplementary Table 2, entry 20), CO is obtained in 83% yield (with 1b formed in 12% yield), suggesting that PdO promotes the oxidation of CO to CO2 (ref. 52). Consequently, it was found that in the presence of PdO, that is, under the standard reaction conditions, the selectivity to CO can be improved to 48% by adding bis(benzene)chromium (Fig. 2b and Supplementary Table 2), with the chlorinated product 1b formed in 72% yield. The product distribution (using PVC and 1a as substrates) was quantified, and confirms that the PVC was completely mineralized into gases (CO and CO2) and the Cl atoms converted into 1b and excess HCl (Supplementary Fig. 12). Moreover, the unpurified gas stream was directly used in the carbonylation of 1-phenylethane-2,3-diol53 (consuming the CO generated) and in the cycloaddition of CO2 to styrene oxide (fixing the CO2 produced) affording styrene carbonate, thereby valorizing all the carbon atoms in PVC (Supplementary Fig. 13).
The depolymerization of PVC was monitored by gel permeation chromatography (GPC) and chromatograms before and after reaction (Fig. 2c) show that the characteristic peaks of PVC (with different molecular weights) completely disappear. Only signals corresponding to small molecules, that is, 1a and 1b, remain, confirming the total depolymerization of the polymers. 1H NMR spectroscopy shows that after the reaction (Fig. 2d; see caption for details of the reaction conditions), the characteristic peaks attributed to the 10-H of substrate 1a and the α/β-Hs of PVC are no longer present, and only signals attributable to the chlorinated product 1b and H2O are observed (for comparison, the 1H NMR spectrum of 1b is provided in Supplementary Fig. 14). The region between 1 and 5 ppm is clear, which is where signals derived from alkyl monomers or oligomers would be expected to be observed. Thus, 1b and water are the only liquid products obtained during the reaction.
Scope of the chlorinated waste
Solid waste derived from commercial chlorinated plastics and rubbers is typically manufactured with other components present, including plasticizers, fillers and pigments, to provide rigidity, elasticity, colour and other properties34. To explore the utility of our method when applied to real waste, a range of postconsumer products were evaluated (Table 1). Using a PVC-based water pipe, electrical conduit and electric wire (P1; Supplementary Fig. 15), chlorinated product 1b was obtained in yields of 80 to 99%. Transparent polyvinylidene chloride (PVDC, P2) is extensively used as a packaging material for food and pharmaceutical products, and in the forms of raw powder and blister affords 1b in 99% yield. Polyepichlorohydrin (PECH, P3) with primary Cl groups was also tested and gave 1b in 99% yield. Rubber has short polymeric chains and extensive cross-linkages, endowing it with greater elasticity than most plastics, but making it more challenging to depolymerize54,55. Nonetheless, neoprene rubber (P4), raw chunks and vacuum tube, both afford 1b in a similar yield, that is, 80–82%, showing that the cross-linkages are transformed under the reaction conditions. Substrate 1a was also chlorinated in the presence of copolymers with hetero-oxygen atoms, that is, poly(epichlorohydrin-co-ethylene oxide) (PECHEO, P5) and poly(epichlorohydrin-co-CO2) (PECHC, P6), with 1b obtained in 99% yield. We simulated real waste streams by employing a mixture of several types of PVC-based and polyolefin (polyethylene (PE) and polypropylene (PP)) plastic waste in the chlorination of 1a under the standard reaction conditions. The polyolefins remain intact after reaction, whereas the PVC was consumed to afford chlorinated product 1b in 87% yield. The use of mixed plastics demonstrates the possibility to selectively valorize PVC from mixtures containing polyolefins and potentially other types of plastic waste, although it is likely that real waste streams would require washing before use, as is common in other plastic upcycling processes56,57.
In addition to plastic waste, various liquid chlorine-containing hydrocarbon wastes were evaluated as chlorination reagents (Table 1). Chlorinated solvents and reagents are extensively used in chemistry and for cleaning purposes in many industries8,9,58. For example, dichloromethane (DCM) is the most extensively used solvent by volume in the pharmaceutical industry (~18%), and requires safe disposal to minimize damage to human health (it is a carcinogen) and damage to the environment. DCM and other commonly used chlorinated solvents (C1 and C4–C8) are good chlorination reagents in our system (40–87%), with the exception of chloroform (C2) and tetrachloromethane (C3). Note that perchloroethene (C8) is the most widely used solvent in dry cleaning58. Other mono- and dichlorinated alkanes (C9 and 10), alkenes (C11) and alkylbenzenes (C13 and 14) serve as excellent sources of chlorine, to afford chlorinated product 1b in 91–99% yield. Chlorocyclohexane (C12) is a poor chlorination reagent, whereas epichlorohydrin (C15) and epichlorohydrin carbonate (C16) perform chlorination well, with both affording 1b in 98% yield.
Actual laboratory waste was used in the reaction, obtained from the synthesis of the ionic liquid 1-butyl-3-methylimidazolium chloride ([BMIM]Cl) prepared from the reaction of excess butyl chloride in DCM (Table 1). Following isolation of the [BMIM]Cl product, the chlorinated waste includes residual butyl chloride and DCM. Using this mixture as the chlorination reagent and performing the reaction on a 5 g scale with respect to 1a, the chlorinated product 1b was obtained in 95% (GC) yield. The pressure and temperature of the reaction were monitored online for a reaction employing 5.4 g of 1a, implying that this is safe to perform when using the appropriate equipment (Supplementary Fig. 16). To further demonstrate the functional group compatibility of this reaction, an additive challenge was performed (Supplementary Table 3)59. We found that only amine additives hinder the activity of our method.
Substrate scope of arenes
Chlorinated arenes are widely employed as pharmaceuticals, agrochemicals, dyes and solvents13,42,60. Chlorination of arenes typically involves toxic and corrosive reagents (sulfuryl dichloride, HCl, Cl2)61,62 or the application of expensive reagents, such as chloramines, which have a low atom economy42,63,64. In contrast, using chlorinated waste as chlorination reagents may be considered as an inexpensive, benign and sustainable method that alleviates problems related to the disposal of such waste. To investigate the scope of this method, a range of aromatic and heteroaromatic substrates with N-directing groups were evaluated using colourless PVC water pipe as the chlorination reagent (Table 2). Pyridine-directing arenes with various electron-withdrawing and electron-donating groups were chlorinated with high selectivity to afford regioselective aryl ortho-dichloride products (2b–7b) or aryl ortho-monochloride products (8b, 9b) in 74–98% yield. The impact of functional groups on the pyridine-directing group (10a, 11a) is critical to control the selectivity of ortho-di- or monochloride products (10b, 11b). Product 12b is an intermediate in the synthesis of vismodegib, a drug used for the treatment of basal cell carcinoma (see ‘Application to pharmaceutical synthesis’ below)65,66. Pyrimidine-directing arenes (13a–18a) also afford the expected chlorinated products, but in slightly lower selectivity of ortho-di- or monochloride products. Interestingly, arenes with pyrazol-directing groups (19a–24a) were selectively monochlorinated in good yield (72–81%). Arenes with 8-aminoquinoline (bidentate, NHQ)-directing groups (25a–30a) were also mono- or dichlorinated, but in slightly lower yields (58–80%). Compounds 25b–27b are important synthetic intermediates of active EP1 antagonists67 and positive allosteric modulators68. In general, the excess PVC employed in the reaction is to ensure high product yields and does not affect the selectivity for ortho-di- or monochloride products. Employing PVC loadings containing stochiometric amounts of chlorine in the reaction slightly decrease the product yield. For example, when employing 12a as substrate (Supplementary Fig. 17), decreasing the PVC loading from 1.5 to 0.75 equiv. decreases the yield of monochloride product from 92% (Cl atom economy 71%) to 65% (Cl atom economy 97%).
Application to pharmaceutical synthesis
This method using Cl-containing waste as a chlorination reagent was applied to the synthesis of the FDA-approved anticancer drug vismodegib (Fig. 3). On the basis of a retrosynthetic analysis of vismodegib, the pyridine-directed arene 12a and NHQ-directed arene 26a were selected as the starting materials66. Ortho-C–H chlorination of 12a followed by reduction gives 4-chloro-3-pyridin-2-ylaniline, 31b. Compound 26a was chlorinated using the standard conditions (see caption to Fig. 3) and hydrolysed to afford 2-chloro-4-(methylsulfonyl)benzoic acid, 32b. Condensation of 31b and 32b affords vismodegib, with an overall yield of 68%. The two Cl groups in vismodegib are derived from the waste PVC water pipe, and the spectroscopic and analytical data (Supplementary Figs. 18–20 and Supplementary Table 4) indicate that the route should be compatible with the stringent purity requirements of the pharmaceutical industry. Green metrics calculations of the process mass intensity (PMI) and environmental factor (E-factor) were performed (Fig. 3), demonstrating that the chlorination method has a similar efficiency and sustainability to a reported C–H chlorination method63.
Mechanistic studies
The reaction mechanism of this reliable and robust chlorination method was probed with a view to establishing the role of the Cu(NO3)2 and PdO catalysts, the NaNO3 promoter and the strong solvent effect of dimethylsulfoxide (DMSO). The reaction may be divided into three parts: (1) dechlorination of chlorinated waste; (2) depolymerization/decomposition of the dechlorinated waste; and (3) chlorination of the arene substrate. Initially, several potential, model chlorination reagents were tested under the standard reaction conditions (Extended Data Fig. 1). Reagents without an α-H and β-H (1c), or chloride salts without H+ (6c, 7c), were inactive or sparingly active (0–8%). Reagents with either an α-H (2c) or β-H (3c) only afforded the chlorinated product 1b in modest yield (46% and 39%, respectively). In contrast, reagents containing both α- and β-H (4c, 5c) provide 1b in good yield (78–90%), which demonstrates that removable α- and β-H are required for chlorination. The application of acetic acid (provides excess H) and NaCl (6c, condition 2) or alternatively HCl (8c) as chlorination reagents notably improves the yield of 1b, further confirming the importance of H (cleavable C–H bonds or H+). These control experiments suggest that in the initial dechlorination step HCl is generated, which acts as the chlorination reagent, and the pH of the reaction mixture confirms the formation of HCl (Supplementary Fig. 21).
Next, the dechlorination of the model reagent 1-phenylethyl chloride (4c) was studied (Extended Data Fig. 2). Using CuO (Extended Data Fig. 2, entry 1) or NaNO3 (Extended Data Fig. 2, entry 2) as the catalyst in DMSO, benzoic acid is the dominant product, revealing simultaneous dechlorination and carbon–carbon bond cleavage. With PdO (Extended Data Fig. 2, entry 3) or without catalyst (Extended Data Fig. 2, entry 4), styrene (obtained by dehydrochlorination) is the main product with 1-phenylethanol (obtained by dechlorohydroxylation) obtained in lower quantities. Dechlorination is not observed in the absence of O2 (Extended Data Fig. 2, entry 5) or in other polar solvents (DMF or tetrahydrofuran (THF); Extended Data Fig. 2, entries 6 and 7). 1H NMR spectroscopy confirms that 4c (used as a model chlorination reagent) interacts with the DMSO solvent, activating the C–Cl bond (Supplementary Fig. 22)69. Hydroxyl radicals were detected by electron paramagnetic resonance spectroscopy during the DMSO/O2-promoted dehydrochlorination process (Supplementary Fig. 23), indicating that dehydrochlorination involves a radical-mediated pathway. Radical trapping and radical clock experiments demonstrate the formation of carbon-centred radicals through the release of Cl• radicals (Supplementary Figs. 24 and 25). These results imply that DMSO/O2 catalyses the dehydrochlorination step to afford HCl16,70,71, with the formation of alkene (dominant) and alkanol (minor) intermediates (the hydroxyl oxygen may originate from O2; Supplementary Fig. 26). The NaNO3 promotes the oxidative decomposition of the dechlorinated (hydrocarbon component) polymer/solvent via C=C/C(OH)–C bond activation of the alkene and alkanol intermediates (Supplementary Figs. 27–29)43,44,45,49. In the final step, the PdO catalyses the chlorination of the arene substrate using HCl as the actual chlorination reagent39,42,72.
Pd-catalysed C–H activation/chlorination was also investigated (Extended Data Fig. 3). Using HCl as the chlorination reagent, chlorination of 1a does not proceed well without additional Cu catalyst and NaNO3 (Extended Data Fig. 3, entries 1–4), which implies that the Cu catalyst and NO3− influence the activity of the Pd catalyst during the oxidative C–H chlorination reaction40,73,74,75. The model benzo[h]quinolinyl Pd(II) chloride intermediate was evaluated under the standard reaction conditions and affords chlorinated product 1b only in the presence of both Cu and NO3− catalysts (Supplementary Fig. 30). X-ray photoelectron spectroscopy was used to confirm that the Cu and NO3− catalysts assist in the oxidation of the Pd catalyst in the presence of O2 (Supplementary Fig. 31). These experiments imply that the Cu and NO3− catalysts act as redox mediators between O2 and Pd(II) intermediates73,75, promoting the formation of Pd(IV) intermediates, followed by reductive elimination to afford chlorinated products39,40,41. A series of tests to establish the nature of the active PdO catalyst was conducted, including hot filtration, elemental analysis, mercury poisoning, Pd(II) trapping and mass spectrometry, with all indicating that the active PdO catalyst is heterogeneous (Supplementary Figs. 32 and 33), although it cannot be excluded that, to a minor extent, the heterogeneous catalyst acts as a reservoir for homogeneous Pd species stabilized by the DMSO solvent76. Notably, without PdO, the combination of Cu(NO3)2 and NaNO3 affords chlorinated product 1b in 25% yield, presumably due to a less favourable Cu-catalysed chlorination pathway involving reduction elimination from a Cu(III) intermediate (Supplementary Fig. 34)77,78.
Taken together, a tentative reaction sequence is shown in Fig. 4. Dechlorination catalysed by DMSO/O2 (a to b) affords alkene and HCl intermediates (Supplementary Fig. 26). The hydrocarbon component undergoes oxidization to CO and H2O via NaNO3-promoted C–C bond cleavage (Supplementary Fig. 29), followed by oxidation of CO to CO2 products (Pd-catalysed mainly). The HCl generated serves as the active chlorination reagent, which generates chlorinated arenes catalysed by the Pd species (c to e; Supplementary Fig. 35). Tentative reaction pathways for PVC- and PVDC-based chlorination reagents are provided in Supplementary Figs. 26, 29 and 34–36.
Life cycle assessment
To evaluate the environmental impact of the chlorination process, life cycle assessment (LCA) modelling was performed and compared with other chlorination strategies, with each system optimized to afford 1 kg of product. Note that the equivalent of PVC is considered to be incinerated for scenarios that do not employ PVC as the chlorination reagent and the production of valuable CO is not included. Details of LCA calculations are provided in Supplementary Figs. 37–40 and Supplementary Tables 5–7. LCA of the common chlorination route39,41 using N-chlorosuccinimide as the chlorination reagent (scenario 1) for the generation of 2-(2-chloro-5-nitrophenyl)pyridine 12b, an intermediate in the synthesis of the anticancer drug vismodegib, produces 9.18 kg of CO2, whereas using PVC as the chlorination reagent (scenario 2), less than six times the amount of CO2 is generated, that is, 1.41 kg, despite the latter route producing CO2 gas as a by-product. The main contribution of the CO2 generated from the N-chlorosuccinimide route consists of the production of the chlorination reagent itself and unrecoverable Pd(OAc)2 catalyst required, whereas using PVC waste is free of charge and the heterogeneous PdO catalyst may be recovered (Supplementary Fig. 11). The PVC route was also compared with the recently published electrochemical chlorination strategy using PVC as a chlorination reagent for the generation of 1 kg of 1-(2-chlorophenyl)-pyrazole 19b (compare scenarios 3 and 4)34. In the electrochemical process, a large excess of PVC and tetrabutylammonium tetrafluoroborate (NBu4BF4) containing electrolyte are needed (the expensive bis(2-ethylhexyl) phthalate additive was not included in the analysis). The LCA indicates that electrochemical chlorination will produce 54.62 kg of CO2, which is over 20 times higher than the method reported here, which would produce 2.59 kg of CO2. The main source of CO2 is from the large quantity of NBu4BF4 electrolyte required. The LCA confirms that the method is more promising and less environmentally detrimental than other reported methods.
Conclusions
More sustainable alternatives to chlorinated compounds are a key goal in green chemistry, although in some cases, for example, in pharmaceutical products79, it is unlikely that replacements will be identified in the near future. The choice of investing in greener chlorination approaches, or finding non-chlorinated alternatives, should be guided by a thorough assessment of the impact on both public health and the environment. Here we have shown that intractable chlorinated waste can be used as chlorination reagents to produce valuable aryl chloride products, with the hydrocarbon component being simultaneously mineralized. A new synthetic route to the FDA-approved drug, vismodegib, was developed, with the two Cl atoms in vismodegib derived from waste PVC water pipe. LCA indicates that this route has a lower environmental impact than the reported chlorination process39,41. Thus, this study charts a path for chlorinated wastes to be ‘decommissioned’ in a safe and sustainable way, simultaneously adding value to the process and additionally eliminating the need to manufacture unsustainable chlorination reagents. Note that chlorine production is the main electricity-consuming process in the chemical industry80 and is not sustainable unless the process is powered by renewable energy, hence using ‘reclaimed’ chlorine is advantageous. Future work will be focused on scaling up the reaction and extending the substrate scope, that is, to arenes without directing groups. Should it prove possible to chlorinate a broader range of arenes using this approach, then substantially larger quantities of chlorinated hydrocarbon waste could be valorized, helping to bridge the gap between chlorinated hydrocarbon waste and its application as chlorination reagents.
Methods
General procedures
7,8-Benzoquinoline 1a (0.25 mmol), PVC water pipe (1.5 equiv., 0.375 mmol), Cu(NO3)2·3H2O (20%, 0.05 mmol), PdO (5%, 0.0125 mmol), NaNO3 (20%, 0.05 mmol), biphenyl (0.2 mmol, internal standard) and DMSO (2 ml) were added into a glass insert vial of the autoclave and charged with O2 (3 bar). The reactor was heated to 140 °C for 15 h. After cooling to room temperature, the gas products were collected with a Tedlar gas-sampling bag (Sigma-Aldrich) for analysis by GC. Ethyl acetate (3 × 3 ml) and an aqueous saturated brine solution (5 ml) was added to the reaction mixture to extract the organic products. The combined organic phase was used for analysis. Further purification was achieved using silica gel chromatography (hexane/ethyl acetate as eluent if not specified) when required.
Analytical methods
Qualitative and quantitative analysis of gas-phase products was performed by GC using an Agilent 7890B instrument equipped with a hydrogen flame-ionization detector and a thermal conductivity detector. The GC yield was determined based on standard gas mixtures and integrated peak areas. Qualitative and quantitative analysis of crude liquid products was performed using an Agilent 7000C GCMS equipped with a hydrogen flame-ionization detector, electron ionization mass detector and HP-5 non-polar column. The GC yield was determined on the basis of internal standard curves and integrated peak areas.
Determination of the molecular weight and polydispersity of the polymers was performed using GPC on an Agilent 390-MDS equipped with a refractive index detector, and dual-angle light scattering detector. THF was used as eluent. For the measurement after reaction, brine (10 ml) was added to the DMSO solution (2 ml) and the organic components were extracted with THF (3 × 5 ml). The THF extract was used for GPC.
1H and 13C NMR spectra were recorded on a Bruker Avance III HD 400 instrument equipped with a 5 mm BBFO probe. DMSO-d6 or CDCl3 were used as solvent. DMSO-d6 was used as the reaction solvent for the reaction that was monitored by 1H NMR spectroscopy. After centrifuging to remove the PdO catalyst, the crude reaction mixture (0.2 ml) was diluted with DMSO-d6 or THF-d8 (0.4 ml) and directly used for the 1H NMR experiment.
Other methods are included in the Supplementary Information.
Data availability
All data generated or analysed during this study are included in this published paper and its Supplementary Information.
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Acknowledgements
This publication was supported by EPFL and was created as part of the NCCR Catalysis (grant no. 180544, P.J.D.), a National Centre of Competence in Research funded by the Swiss National Science Foundation. We thank M. Hua and D. Savary for helpful discussions and B. Ding for performing X-ray photoelectron spectroscopy experiments.
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M.L. and P.J.D. designed the research, analysed data and wrote the paper. M.L. and X.W. performed the research.
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The catalytic method is described in a patent invented by M.L. and P.J.D. (EP patent, No. 23170105.3). The other authors declare no competing interests.
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Extended data
Extended Data Fig. 1 Application of model organic and inorganic chlorides as chlorination reagents.
Standard conditions: (1) 7,8-benzoquinoline 1a (0.25 mmol), chlorides (1.5 equiv., 0.375 mmol), Cu(NO3)2•3H2O (20 mol%, 0.05 mmol), PdO (5 mol%, 0.0125 mmol), NaNO3 (20 mol%, 0.05 mmol), biphenyl (0.2 mmol, internal standard), DMSO (2 mL), O2 (3 bar), 140 °C, 15 h. (2) with acetic acid (3 equiv., 0.75 mmol). (3) with HCl (3 equiv., 0.75 mmol).
Extended Data Fig. 2 Evaluation of dechlorination and C=C/C(OH)−C bond activation using model compound 4c.
Reaction conditions: substrate 4c (0.25 mmol), catalyst (20 mol%, 0.05 mmol), solvent (2 mL), biphenyl (0.2 mmol), gas (1 bar), 140 °C, 3 h.
Extended Data Fig. 3 Optimization of the chlorination reaction using HCl as a chlorination reagent.
Standard conditions: 7,8-benzoquinoline 1a (0.25 mmol), HCl (3 equiv., 0.75 mmol), Cu(NO3)2•3H2O (20 mol%, 0.05 mmol), PdO (5 mol%, 0.0125 mmol), NaNO3 (20 mol%, 0.05 mmol), biphenyl (0.2 mmol, internal standard), DMSO (2 mL), O2 (3 bar), 140 °C, 15 h.
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Supplementary figures, tables, materials and methods, life cycle assessment, NMR spectra and references.
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Liu, M., Wu, X. & Dyson, P.J. Tandem catalysis enables chlorine-containing waste as chlorination reagents. Nat. Chem. 16, 700–708 (2024). https://doi.org/10.1038/s41557-024-01462-8
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DOI: https://doi.org/10.1038/s41557-024-01462-8
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