ACRIDINIUM-BASED PHOTOREDOX CATALYSTS, SYNTHESIS AND USE THEREOF IN OXIDATIVE CLEAVAGE OF C-O BONDS

Abstract

The present invention belongs to the field of catalytic chemistry, and more specifically to catalysed oxidation of lignin. It also relates to synthesis of catalyst compounds.

The present invention relates to new acridinium-based photoredox catalyst compounds and their use thereof in a chemical reaction, preferably in depolymerisation of lignin models and ultimately lignin. The invention also relates to the method of synthesis of the new acridinium-based photoredox catalyst compounds according to the invention.

Claims

1. A compound of formula I: ##STR00026## wherein the R.sup.1 and R.sup.2 groups independently represents H, a halo group or a phenyl group, the R.sup.3 group represents H, a halo group, a C1 to C4 linear or branched alkyl chain, a —CN group, a —COOR group, a —COR group or a phenyl group, in which R represents a C1 to C4 linear or branched alkyl chain, and X.sup.− represents an anion.

2. The compound according to claim 1, wherein R.sup.3 is not H, Cl or Me when R.sup.1 and R.sup.2 are H.

3. A compound of formula II: ##STR00027## wherein the R.sup.1 group represents a halo group or a phenyl group; and X.sup.− represents an anion.

4. A compound of formula III: ##STR00028## wherein, the R.sup.3 group represents a halo group, a C1 to C4 linear or branched alkyl chain, a —CN group, a —COOR group a —COR group or a phenyl group, wherein R is a C1 to C4 linear or branched alkyl chain, and X.sup.− represents an anion.

5. A compound of formula IV: ##STR00029## wherein, the R.sup.1 group represents a halo group or a phenyl group, the R.sup.3 group represents a halo group, a C1 to C4 linear or branched alkyl chain, a —CN group, a —COOR group a —COR group or a phenyl group, in which R is a C1 to C4 linear or branched alkyl chain, and X.sup.− represents an anion.

6. The compound according to claim 1, wherein the anion X.sup.− is selected from the group comprising consisting of BF.sub.4.sup.−, PF.sub.6.sup.−, Cl.sup.−, and ClO.sub.4.sup.−.

7. A method of C—O bond cleavage or a photocatalytic C—O bond cleavage comprising using the compound of claim 1.

8. A method for lignin depolymerisation or oxidative depolymerisation of lignin comprising irradiating lignin or a lignin model, in an organic solvent, in the presence of a compound of claim 1.

9. A synthetic method of making a compound of formula I comprising a step of photoreacting, in an organic solvent, a 10-methylacridinium salt and a diazonium salt of formula I′: ##STR00030## wherein, the R.sup.1 and R.sup.2 groups independently represent H, a halo group or a phenyl group, the R.sup.3 group represents H, a halo group, a C1 to C4 linear or branched alkyl chain, a —CN group, a —COOR group, a —COR group or a phenyl group, in which R represents a C1 to C4 linear or branched alkyl chain, and X.sup.− represents an anion.

10. The method according to claim 9, wherein at least one group among of R.sup.1, R.sup.2 or R.sup.3 is not H.

11. The method according to claim 8, wherein the anion X.sup.− is selected from the group consisting of BF.sub.4.sup.−, PF.sub.6.sup.−, Cl.sup.− and ClO.sub.4.sup.−.

12. The method according to claim 8, wherein the compounds of formula I′ are selected from compounds of formula II′: ##STR00031## wherein R.sup.1 represents a halo group or a phenyl group, and X.sup.− represents an anion.

13. The method according to claim 8, wherein the compounds of formula I′ are selected from compounds of formula III′: ##STR00032## wherein, the R.sup.3 group represents a halogen, a C1 to C4 linear or branched alkyl chain, a —CN group, a —COOR group, a —COR group or a phenyl group, wherein R is a C1 to C4 linear or branched alkyl chain; and X.sup.− represents an anion.

14. The method according to claim 8, wherein the compounds of formula I′ are selected from compounds of formula IV′: ##STR00033## wherein, the R.sup.1 group represents a halo group or a phenyl group, the R.sup.3 group represents a halo group, a C1 to C4 linear or branched alkyl chain, a —CN group, a —COOR group a —COR group or a phenyl group, in which R is a C1 to C4 linear or branched alkyl chain, and X.sup.− represents an anion.

15. The method according to claim 8, wherein the organic solvent is selected from the group consisting of methanol, dimethylsulfoxide, acetonitrile, dichloromethane and mixtures thereof.

16. The method according to claim 8, wherein the 10-methylacridinium salt is selected from the group consisting of BF.sub.4.sup.−, PF.sub.6.sup.−, Cl.sup.− and ClO.sub.4.sup.−.

17. The method according to claim 8, wherein the photoreaction is done by means of irradiation at a wavelength comprised in the range of visible light, preferably from 400 to 800 nm, and more preferably from 440 to 460 nm.

18. The method according to claim 8, wherein the reaction is done at a temperature in a range from 10 to 45° C.

19. The compound according to claim 6, wherein the anion X.sup.− is BF.sub.4.sup.−.

20. The method according to claim 11, wherein the anion X.sup.− is BF.sub.4.sup.−.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0009] Applicant has developed new catalyst compounds that solves all of the problems listed above.

[0010] The present invention deals with acridinium-based photoredox catalyst compounds, their synthetic methods and their applications, such as depolymerisation of lignin.

[0011] The catalyst of the invention presents the advantage to be easily synthesised, in mild conditions and present a photoredox catalytic activity for the oxidative C—O bond cleavage of lignin model compounds without peroxidation step activity that is superior to known catalysts, in particular superior to the most commonly used, such as the Fukuzumi catalyst.

[0012] The invention therefore relates to a compound of formula I:

##STR00001## [0013] wherein, [0014] the R.sup.1 and R.sup.2 groups independently represent H, a halo group or a phenyl group, [0015] the R.sup.3 group represents H, a halo group, a C1 to C4 linear or branched alkyl chain, a —CN group, a —COOR group, a —COR group or a phenyl group, in which R represents a C1 to C4 linear or branched alkyl chain, and [0016] X.sup.− represents an anion.

[0017] Advantageously, the compound according to the invention may be chosen from the compounds of formula I:

##STR00002## [0018] wherein: [0019] the R.sup.1 and R.sup.2 groups independently represent H, a halo group or a phenyl group, [0020] the R.sup.3 group represents H, a halo group, a C1 to C4 linear or branched alkyl chain, a —COOR group, a —COR group or a phenyl group, in which R represents a C1 to C4 linear or branched alkyl chain, and [0021] X.sup.− represents an anion.

[0022] It is meant by a “halo group”, a group derived from a halogen. Preferably, the halogen may be chosen in the group comprising fluorine, chlorine, bromine or iodine, preferably bromine or iodine. The halo group may thus be chosen in the group comprising fluoro, chloro, bromo or iodo group, preferably bromo or iodo group.

[0023] Advantageously, the R.sup.1 and R.sup.2 groups independently represents H, a halo group or a phenyl group. Preferably, the R.sup.1 and R.sup.2 groups may independently represent H, a bromo, a iodo or a phenyl group.

[0024] Advantageously, the R.sup.3 group represents H, a halo group, a C1 to C4 linear or branched alkyl chain, a —CN group, a —COOR group, a —COR group or a phenyl group, in which R represents a C1 to C4 linear or branched alkyl chain. The R.sup.3 group may represent H, a halo group, a C1 to C4 linear or branched alkyl chain, a —COOR group, a —COR group or a phenyl group, in which R represents a C1 to C4 linear or branched alkyl chain. Preferably, the R.sup.3 group represents H, a halo group, a C2 to C4 linear or branched alkyl chain, a —CN group, a —COOR group, a —COR group or a phenyl group, in which R represents a C1 to C4 linear or branched alkyl chain. Preferably, the R.sup.3 group may represent H, a bromo group, -COOEt, —COMe or Me. More preferably, the R.sup.3 group may represent H, a bromo group, -COOEt, or —COMe.

[0025] Advantageously, the compound according to the invention may be a compound of formula I wherein at least one group amongst R.sup.1, R.sup.2 and R.sup.3 is not H.

[0026] Advantageously, the compound according to the invention may be a compound of formula I wherein R.sup.3 is not H, F Cl or Me when R.sup.1 and R.sup.2 are H.

[0027] Advantageously, the compound according to the invention may be a compound of formula I wherein R.sup.1 may be H, a bromo, a iodo or a phenyl group, R.sup.2 may be H and R.sup.3 may be H, a bromo group, -COOEt, —COMe or Me, and R.sup.1 and R.sup.3 may not be H simultaneously.

[0028] Advantageously, the compound according to the invention may be a compound of formula I wherein R.sup.1 may be H, a bromo, a iodo or a phenyl group, R.sup.2 may be H and R.sup.3 may be H, a bromo group, -COOEt, —COMe, and R.sup.1 and R.sup.3 may not be H simultaneously.

[0029] Advantageously, the compound according to the invention may be chosen from the compounds of formula I wherein R.sup.2 and R.sup.3 are H, of formula II. The compound may be of formula II:

##STR00003## [0030] wherein, [0031] the R.sup.1 group represents a halo group or a phenyl group, and [0032] X.sup.− represents an anion. Preferably, R.sup.1 may be a bromo or a iodo group.

[0033] Advantageously, the compound according to the invention may be chosen from the compounds of formula I wherein R.sup.1 and R.sup.2 are H, of formula III. The compound may be of formula III:

##STR00004## [0034] wherein, [0035] the R.sup.3 group represents a halo group, a C1 to C4 linear or branched alkyl chain, a —CN group, a —COOR group a —COR group or a phenyl group, in which R is a C1 to C4 linear or branched alkyl chain, and [0036] X.sup.− represents an anion. Preferably, the R.sup.3 group represents a halo group, a C2 to C4 linear or branched alkyl chain, a —CN group, a —COOR group a —COR group or a phenyl group, in which R is a C1 to C4 linear or branched alkyl chain.

[0037] Advantageously, the compound according to the invention may be chosen from the compounds of formula I wherein R.sup.1 and R.sup.2 are H, of formula III. The compound may be of formula III:

##STR00005## [0038] wherein, [0039] the R.sup.3 group represents a halo group, a C1 to C4 linear or branched alkyl chain, a —COOR group a —COR group or a phenyl group, in which R is a C1 to C4 linear or branched alkyl chain, and [0040] X.sup.− represents an anion. Preferably, R.sup.3 may be a bromo group, -COOEt, —COMe or Me. More preferably, R.sup.3 may be a bromo group, -COOEt or —COMe.

[0041] Advantageously, the compound according to the invention may be chosen from the compounds of formula I wherein R.sup.2 is H, of formula IV. The compound may be of formula IV:

##STR00006## [0042] wherein, [0043] the R.sup.1 group represents a halo group or a phenyl group, [0044] the R.sup.3 group represents a halo group, a C1 to C4 linear or branched alkyl chain, a —CN group, a —COOR group a —COR group or a phenyl group, in which R is a C1 to C4 linear or branched alkyl chain, and [0045] X.sup.− represents an anion. Preferably, R.sup.1 may be a bromo group. Preferably, R.sup.3 may be a fluoro group, a bromo group, a chloro group, —CN, —COOMe, -COOEt, —COMe or Me. More preferably, R.sup.1 may be a bromo group and R.sup.3 may be a fluoro group, a bromo group, a chloro group, —CN, —COOMe, -COOEt, —COMe or Me.

[0046] Advantageously, the compound according to the invention may be chosen in the group of compounds of formula I, II, III or IV wherein the anion X.sup.− is chosen in the group comprising tetraborate (BF.sub.4.sup.−), hexafluorophosphate (PF.sub.6.sup.−), chloride (Cl.sup.−) and perchlorate (ClO.sub.4.sup.−), preferably BF.sub.4.sup.−.

[0047] Advantageously, the compound according to the invention may be chosen in the group of compounds of formula I, II, or III wherein the anion X.sup.− is chosen in the group comprising tetraborate (BF.sub.4.sup.−), hexafluorophosphate (PF.sub.6.sup.−), chloride (Cl) and perchlorate (ClO.sub.4.sup.−), preferably BF.sub.4.sup.−.

[0048] Advantageously, the compound according to the invention may be chosen in the following group of compounds:

##STR00007## ##STR00008##

[0049] The invention further relates to a use of a compound according to the invention as a catalyst, preferably in a C—O bond cleavage reaction, and more preferably a photocatalytic C—O bond cleavage.

[0050] Advantageously, the use according to the invention may be the use of a compound according to the invention in a reaction of lignin depolymerisation, preferably in oxidative depolymerisation of lignin.

[0051] Advantageously, the invention may relate to a method of C—O bond cleavage, preferably a method of photocatalytic C—O bond cleavage comprising a step of using a compound according to the invention.

[0052] Advantageously, the invention may relate to a reaction of lignin depolymerisation, preferably an oxidative depolymerisation of lignin, comprising a step of using a compound according to the invention.

[0053] Advantageously, in the method or use according to the invention, the C—O bond cleavage reaction or the reaction of lignin depolymerisation may be done, by irradiation of lignin or a lignin model, in an organic solvent, in the presence of a compound according to the invention. The organic solvent may be chosen in the group comprising methanol (MeOH), dimethylsulfoxide (DMSO), acetonitrile (ACN), dichloromethane (DCM) and mixtures thereof. The C—O bond cleavage reaction or the reaction of lignin depolymerisation may be done by photoreacting lignin or a lignin model in the presence of a compound according to the invention by means of irradiation at a wavelength comprised in the range of visible light (i.e. from 400 to 800 nm), preferably from 440 to 460 nm. The source of light may be a LED, preferably a blue light LED. Irradiation may last from 6 hours to 20 hours, preferably 12 hours. The C—O bond cleavage reaction or the reaction of lignin depolymerisation may be done at a temperature comprised in a range from 10 to 45° C., preferably 30° C.

[0054] Advantageously, in the method or use according to the invention, the C—O bond cleavage reaction or the reaction of lignin depolymerisation may be done under an 02 atmosphere or under an air atmosphere.

[0055] The invention also relates to a synthetic method of a compound of formula I comprising a step of photoreacting, in an organic solvent, a 10-methylacridinium salt and a diazonium salt of formula I′:

##STR00009## [0056] wherein, [0057] the R.sup.1 and R.sup.2 groups independently represent H, a halo group or a phenyl group, [0058] the R.sup.3 group represents H, a halo group, a C1 to C4 linear or branched alkyl chain, a —CN group, a —COOR group, a —COR group or a phenyl group, in which R represents a C1 to C4 linear or branched alkyl chain, and [0059] X.sup.− represents an anion.

[0060] Advantageously, the invention may also relate to a synthetic method of a compound of formula I comprising a step of photoreacting, in an organic solvent, a 10-methylacridinium salt and a diazonium salt of formula I′:

##STR00010## [0061] wherein, [0062] the R.sup.1 and R.sup.2 groups independently represent H, a halo group or a phenyl group, [0063] the R.sup.3 group represents H, a halo group, a C1 to C4 linear or branched alkyl chain, a —COOR group, a —COR group or a phenyl group, in which R represents a C1 to C4 linear or branched alkyl chain, and [0064] X.sup.− represents an anion.

[0065] Advantageously, the R.sup.1 and R.sup.2 groups independently represents H, a halo group or a phenyl group. Preferably, the R.sup.1 and R.sup.2 groups may independently represent H, a bromo, a iodo or a phenyl group.

[0066] Advantageously, the R.sup.3 group represents H, a halo group, a C1 to C4 linear or branched alkyl chain, a —CN group, a —COOR group, a —COR group or a phenyl group, in which R represents a C1 to C4 linear or branched alkyl chain. The R.sup.3 group may represent H, a halo group, a C1 to C4 linear or branched alkyl chain, a —COOR group, a —COR group or a phenyl group, in which R represents a C1 to C4 linear or branched alkyl chain. Preferably, the R.sup.3 group represents H, a halo group, a C2 to C4 linear or branched alkyl chain, a —COOR group, a —CN group, a —COR group or a phenyl group, in which R represents a C1 to C4 linear or branched alkyl chain. Preferably, the R.sup.3 group may H, a bromo group, -COOEt, —COMe or Me. More preferably, the R.sup.3 group may represent H, a bromo group, -COOEt, or —COMe.

[0067] Advantageously, the synthetic method according to the invention may be a synthetic method of a compound of formula I comprising a step of photoreacting, in an organic solvent, a 10-methylacridinium salt and a diazonium salt of formula I′, wherein R.sup.3 is not H, F Cl or Me when R.sup.1 and R.sup.2 are H.

[0068] Advantageously, the synthetic method according to the invention may be a synthetic method of a compound of formula I comprising a step of photo reacting, in an organic solvent, a 10-methylacridinium salt and a diazonium salt of formula I′, wherein R.sup.1 may be H, a bromo, a iodo or a phenyl group, R.sup.2 may be H and R.sup.3 may be H, a bromo group, -COOEt, —COMe or Me, and R.sup.1 and R.sup.3 may not be H simultaneously.

[0069] Advantageously, the synthetic method according to the invention may be a synthetic method of a compound of formula I comprising a step of photo reacting, in an organic solvent, a 10-methylacridinium salt and a diazonium salt of formula I′, wherein R.sup.1 may be H, a bromo, a iodo or a phenyl group, R.sup.2 may be H and R.sup.3 may be H, a bromo group, -COOEt, —COMe, and R.sup.1 and R.sup.3 may not be H simultaneously.

[0070] Advantageously, the synthetic method according to the invention may be a synthetic method of a compound of formula I comprising a step of photo reacting, in an organic solvent, a 10-methylacridinium salt and a diazonium salt of formula I′, wherein at least one group amongst R.sup.1, R.sup.2 and R.sup.3 is not H.

[0071] Advantageously, the invention may also relate to a synthetic method of a compound of formula II comprising a step of photoreacting, in an organic solvent, a 10-methylacridinium salt and a diazonium salt of formula II′:

##STR00011## [0072] wherein [0073] the R.sup.1 group represents a halo group or a phenyl group, and [0074] X.sup.− represents an anion. Preferably, R.sup.1 may be a bromo or a iodo group.

[0075] Advantageously, the invention may also relate to a synthetic method of a compound of formula III comprising a step of photoreacting, in an organic solvent, a 10-methylacridinium salt and a diazonium salt of formula III′:

##STR00012## [0076] wherein, [0077] the R.sup.3 group represents a halo group, a C1 to C4 linear or branched alkyl chain, a —CN group, a —COOR group, a —COR group or a phenyl group, in which R is a C1 to C4 linear or branched alkyl chain, and [0078] X.sup.− represents an anion. Preferably, the R.sup.3 group represents a halo group, a C2 to C4 linear or branched alkyl chain, a —CN group, a —COOR group a —COR group or a phenyl group, in which R is a C1 to C4 linear or branched alkyl chain.

[0079] Advantageously, the invention may also relate to a synthetic method of a compound of formula III comprising a step of photoreacting, in an organic solvent, a 10-methylacridinium salt and a diazonium salt of formula III′:

##STR00013## [0080] wherein, [0081] the R.sup.3 group represents a halo group, a C1 to C4 linear or branched alkyl chain, a —COOR group, a —COR group or a phenyl group, in which R is a C1 to C4 linear or branched alkyl chain, and [0082] X.sup.− represents an anion. Preferably, R.sup.3 may be a bromo group, -COOEt, —COMe or Me. More preferably, R.sup.3 may be a bromo group, -COOEt or —COMe.

[0083] Advantageously the invention may also relate to a synthetic method of a compound of formula IV comprising a step of photoreacting, in an organic solvent, a 10-methylacridinium salt and a diazonium salt of formula IV′:

##STR00014## [0084] wherein, [0085] the R.sup.1 group represents a halo group or a phenyl group, [0086] the R.sup.3 group represents a halo group, a C1 to C4 linear or branched alkyl chain, a —CN group, a —COOR group a —COR group or a phenyl group, in which R is a C1 to C4 linear or branched alkyl chain, and [0087] X.sup.− represents an anion. Preferably, R.sup.1 may be a bromo group. Preferably, R.sup.3 may be a fluoro group, a bromo group, a chloro group, —CN, —COOMe, -COOEt, —COMe or Me. More preferably, R.sup.1 may be a bromo group and R.sup.3 may be a fluoro group, a bromo group, a chloro group, —CN, COOMe, -COOEt, —COMe or Me.

[0088] Advantageously, in the synthetic method according to the invention, the compound may be chosen from the compounds of formula I′, II′ or III′ wherein the anion X.sup.− is chosen in the group comprising tetraborate (BF.sub.4.sup.−), hexafluorophosphate (PF.sub.6.sup.−), chloride (Cl.sup.−) and perchlorate (ClO.sub.4.sup.−), preferably BF.sub.4.sup.−.

[0089] Advantageously, in the synthetic method according to the invention, the step of photoreacting a 10-methylacridinium salt and a diazonium salt of formula I′, II′ or III′ is carried out in an organic solvent. The organic solvent may be chosen in the group comprising methanol (MeOH), dimethylsulfoxide (DMSO), acetonitrile (ACN), dichloromethane (DCM) and mixtures thereof. The concentration of 10-methyl-9-phenylacridinium salt may be from 0.12 to 1.2 mol/L. The concentration of diazonium salt may be from 0.1 to 1 mol/L.

[0090] Advantageously, the 10-methylacridinium salt may be chosen in the group comprising 10-methylacridinium tetra borate (BF.sub.4.sup.−), 10-methylacridinium hexafluorophosphate (PF.sub.6.sup.−), 10-methylacridinium chloride (Cl) and 10-methylacridinium perchlorate (ClO.sub.4.sup.−), preferably 10-methylacridinium tetraborate.

[0091] Advantageously, in the synthetic method according to the invention, the step of photoreacting a 10-methylacridinium salt and a diazonium salt of formula I′, II′ or III′ may be done by means of irradiation at a wavelength comprised in the range of visible light (i.e. from 400 to 800 nm), preferably from 440 to 460 nm. The source of light may be a LED, preferably a blue light LED. Irradiation may last from 30 minutes to 2 hours, preferably 1 hour.

[0092] Advantageously, in the synthetic method according to the invention, the step of photoreacting a 10-methylacridinium salt and a diazonium salt of formula I′, II′ or III′ may be done at a temperature comprised in a range from 10 to 45° C., preferably 30° C.

[0093] Advantageously, the synthetic method may further comprise a step of quenching the reaction by addition of an organic solvent (preferably CH.sub.2Cl.sub.2). The quenching of the reaction may be followed by a step of washing the crude mixture with water and removing the solvent under reduced pressure. The obtained catalyst compound may be further purified by flash column chromatography on silica gel.

Examples

Example 1: Preparation of OPC1-8 According to the Invention

[0094] All reactions were carried out under argon atmosphere with standard Schlenk techniques. All reagents were obtained from commercial sources and used as supplied. Technical grade petroleum ether (40-60) and ethyl acetate were used for column chromatography. .sup.1H NMR spectra were recorded on Bruker GPX (300, 400 or 500 MHz) spectrometer. Chemical shifts (δ) were reported in parts per million relative to residual chloroform (7.28 ppm for 1 H; 77.23 ppm for 13C), constants were reported in Hertz. .sup.1H NMR assignment abbreviations were the following: singlet (s), doublet (d), triplet (t), quartet (q), doublet of doublets (dd), doublet of triplets (dt), and multiplet (m). 13C NMR spectra were recorded at 100 MHz on the same spectrometer and reported in ppm. GC-analyses were performed with a GC-2010 (Shimadzu) instrument equipped with a 30 m capillary column (Agilent J&W DB-FFAP, 15 m×0,250 mm×0.25 μm), which was used with helium as the vector gas. The following GC conditions were used: initial temperature 80° C. for 5 minutes, then rate 20° C./min until 280° C. and 280° C. for 28 minutes. HRMS were recorded on a Waters Q-Tof 2 mass spectrometer at the corresponding facilities of the CRMPO, Centre Régional de Mesures Physiques de l'Ouest, Université de Rennes 1.

General Procedure for the Preparation of Acridinium-Based Photoredox Catalysts (OPC Compounds):

[0095] To a 25 mL Schlenk tube was added 10-methylacridinium tetrafluoroborate (168 mg, 0.6 mmol, 1.2 equiv), and diazonium salts (0.5 mmol, 1 equiv) under air. The air was evacuated and backfilled with argon (3 times). Freshly distilled DMSO (1 mL) and MeOH (1 mL) was added. The Schlenk tube was then sealed under argon with a Teflon lined cap. The Schlenk was positioned on a stir plate approximately 2-3 cm from two ABI PAR38 (24\A) LED lamp supplying blue light (λ=440-460 nm). Fans were used to maintain the temperature around 30° C. After 1 hour irradiation, the reaction was quenched by addition of 20 ml CH.sub.2Cl.sub.2 and the crude mixture was washed with 3 mL cold water 3 times, then the solvent was removed under reduced pressure and purified by flash column chromatography on silica gel/Al.sub.2O.sub.3 to give pure product. Results are presented in table 1 below.

##STR00015##

TABLE-US-00001 TABLE 1 OPC compounds yields (%) based on diazonium salt. Yields (%) 10- R.sup.1= based on OPC methylacridinium R.sup.2= diazonium compound tetrafluoroborate diazonium salt R.sup.3= salt OPC1 0.6 mmol 0.5 mmol R.sup.1 = H 80 R.sup.2 = H R.sup.3 = H OPC2 0.6 mmol 0.5 mmol R.sup.1 = H 68 R.sup.2 = H R.sup.3 = Br OPC3 0.6 mmol 0.5 mmol R.sup.1 = H 65 R.sup.2 = H R.sup.3 = COOEt OPC4 0.6 mmol 0.5 mmol R.sup.1 = H 71 R.sup.2 = H R.sup.3 = COMe OPC5 0.6 mmol 0.5 mmol R.sup.1 = Br 58 R.sup.2 = H R.sup.3 = H OPC6 0.6 mmol 0.5 mmol R.sup.1 = I 57 R.sup.2 = H R.sup.3 = H OPC7 0.6 mmol 0.5 mmol R.sup.1 = Ph 79 R.sup.2 = H R.sup.3 = H OPC8 0.6 mmol 0.5 mmol R.sup.1 = Br 56 R.sup.2 = H R.sup.3 = Me

##STR00016##

10-Methyl-9-phenylacridinium tetrafluoroborate (OPC1)

[0096] Following the general procedure using phenyl diazonium tetrafluoroborate (96 mg, 0.5 mmol), the residue was purified by flash chromatography on silica gel to afford the desired compound OPC1 (143 mg, 80%) as a yellow solid. .sup.1H NMR (400 MHz, Acetone-d.sub.6) δ 8.94 (d, J=9.3 Hz, 2H), 8.64-8.47 (m, 2H), 8.10 (d, J=8.5 Hz, 2H), 8.05-7.96 (m, 2H), 7.82 (dd, J=4.9, 1.7 Hz, 3H), 7.66 (dd, J=6.4, 3.0 Hz, 2H), 5.15 (s, 3H). .sup.11B NMR (128 MHz, Acetone-d.sub.6) δ-0.90. .sup.13C NMR (101 MHz, Acetone-d.sub.6) δ 162.4, 142.6, 139.5, 134.2, 131.1, 130.9, 130.7, 129.7, 128.7, 127.0, 119.6, 39.5. .sup.19F NMR (376 MHz, Acetone-d.sub.6) δ-151.86.

##STR00017##

9-(4-Bromophenyl)-10-methylacridinium tetrafluoroborate (OPC2)

[0097] Following the general procedure using 4-bromobenzenediazonium tetrafluoroborate (135 mg, 0.5 mmol), the residue was purified by flash chromatography on silica gel to afford the desired compound OPC2 (148 mg, 68%) as a yellow solid. .sup.1H NMR (400 MHz, Acetone-d.sub.6) δ 8.95 (d, J=9.2 Hz, 2H), 8.59-8.47 (m, 2H), 8.13 (d, J=8.5 Hz, 2H), 8.07-7.93 (m, 4H), 7.63 (d, J=8.2 Hz, 2H), 5.14 (s, 3H). .sup.11B NMR (128 MHz, Acetone-d.sub.6) δ-0.94. .sup.13C NMR (101 MHz, Acetone-d.sub.6) δ 160.9, 142.6, 139.6, 133.4, 132.9, 132.7, 130.7, 128.8, 126.8, 125.0, 119.7, 39.6. .sup.19F NMR (376 MHz, Acetone-d.sub.6) δ-151.80. HRMS (ESI) (m/z): [M].sup.+ calcd. For C.sub.20H.sub.15N.sup.79Br: 348.0382, found: 348.0380.

##STR00018##

9-(4-(Ethoxycarbonyl)phenyl)-10-methylacridinium tetrafluoroborate (OPC3)

[0098] Following the general procedure using 4-(ethoxycarbonyl)benzenediazonium tetrafluoroborate (132 mg, 0.5 mmol), the residue was purified by flash chromatography on silica gel to afford the desired compound OPC3 (139 mg, 65%) as a yellow solid. .sup.1H NMR (400 MHz, Methylene Chloride-d.sub.2) δ 8.66 (d, J=9.2 Hz, 2H), 8.47-8.35 (m, 4H), 8.02-7.95 (m, 2H), 7.90-7.80 (m, 2H), 7.61 (d, J=8.3 Hz, 2H), 4.99 (s, 3H), 4.48 (q, J=7.1 Hz, 2H), 1.47 (t, J=7.1 Hz, 3H). .sup.11B NMR (128 MHz, Methylene Chloride-d.sub.2) δ-1.20. .sup.13C NMR (101 MHz, Methylene Chloride-d.sub.2) δ 165.3, 160.5, 141.4, 139.2, 137.0, 132.6, 129.9, 129.9, 129.8, 128.0, 125.7, 118.3, 61.6, 39.0, 14.0. .sup.19F NMR (376 MHz, Methylene Chloride-d.sub.2) δ-153.04. HRMS (ESI) (m/z): [M].sup.+ calcd. For C.sub.23H.sub.20NO.sub.2.sup.−: 342.1488, found: 342.1492.

##STR00019##

9-(4-Acetylphenyl)-10-methylacridinium tetrafluoroborate (OPC4)

[0099] Following the general procedure using 4-acetylbenzenediazonium tetrafluoroborate (117 mg, 0.5 mmol), the residue was purified by flash chromatography on silica gel to afford the desired compound OPC4 (106 mg, 71%) as a green solid. .sup.1H NMR (400 MHz, Methylene Chloride-d.sub.2) δ 8.66 (d, J=9.2 Hz, 2H), 8.47-8.36 (m, 2H), 8.29 (d, J=8.2 Hz, 2H), 7.99 (d, J=9.4 Hz, 2H), 7.93-7.79 (m, 2H), 7.64 (d, J=8.3 Hz, 2H), 4.98 (s, 3H), 2.75 (s, 3H). .sup.11B NMR (128 MHz, Methylene Chloride-d.sub.2) δ-1.19. .sup.13C NMR (101 MHz, Methylene Chloride-d.sub.2) δ 197.5, 160.9, 142.0, 139.8, 139.1, 137.7, 130.7, 130.43, 129.1, 128.6, 126.2, 118.9, 39.5, 27.1. .sup.19F NMR (376 MHz, Methylene Chloride-d.sub.2) δ-152.81. HRMS (ESI) (m/z): [M].sup.+ calcd. For C.sub.22H.sub.18NO: 312.1383, found: 312.1380.

##STR00020##

9-(2-Bromophenyl)-10-methylacridinium tetrafluoroborate (OPC5)

[0100] Following the general procedure using 2-bromobenzenediazonium tetrafluoroborate (135 mg, 0.5 mmol), the residue was purified by flash chromatography on silica gel to afford the desired compound OPC5 (126 mg, 58%) as a yellow solid. .sup.1H NMR (400 MHz, Methylene Chloride-d.sub.2) δ 8.68 (d, J=9.2 Hz, 2H), 8.52-8.31 (m, 2H), 8.14-7.79 (m, 5H), 7.76-7.62 (m, 2H), 7.48-7.36 (m, 1H), 5.00 (s, 3H). .sup.11B NMR (128 MHz, Methylene Chloride-d.sub.2) δ-1.13. .sup.13C NMR (101 MHz, Methylene Chloride-d.sub.2) δ 159.9, 141.5, 139.3, 133.9, 133.4, 132.1, 131.1, 129.6, 128.3, 128.1, 125.7, 122.2, 118.4, 39.0. .sup.19F NMR (376 MHz, Methylene Chloride-d.sub.2) δ-152.96. HRMS (ESI) (m/z): [M].sup.+ calcd. For C.sub.20H.sub.15N.sup.79Br: 348.0382, found: 348.0383.

##STR00021##

9-(2-Iodophenyl)-10-methylacridin-10-ium tetrafluoroborate (OPC6)

[0101] Following the general procedure using 2-iodobenzenediazonium tetrafluoroborate (159 mg, 0.5 mmol), the residue was purified by flash chromatography on silica gel to afford the desired compound OPC6 (138 mg, 57%) as a yellow solid. .sup.1H NMR (400 MHz, Methylene Chloride-d.sub.2) δ 8.67 (d, J=9.3 Hz, 2H), 8.52-8.35 (m, 2H), 8.20 (d, J=8.6 Hz, 1H), 7.86 (d, J=4.1 Hz, 4H), 7.77-7.68 (m, 1H), 7.52-7.33 (m, 2H), 4.98 (s, 3H). .sup.11B NMR (128 MHz, Methylene Chloride-d.sub.2) δ-1.15. .sup.13C NMR (101 MHz, Methylene Chloride-d.sub.2) δ 162.3, 141.6, 139.8, 139.3, 138.0, 131.8, 130.4, 129.7, 128.7, 128.2, 125.6, 118.4, 96.6, 39.0. .sup.19F NMR (376 MHz, Methylene Chloride-d.sub.2) δ-152.88.

##STR00022##

9-([1,1′-Biphenyl]-2-yl)-10-methylacridinium tetrafluoroborate (OPC7)

[0102] Following the general procedure using 2-phenylbenzenediazonium tetrafluoroborate (134 mg, 0.5 mmol), the residue was purified by flash chromatography on silica gel to afford the desired compound OPC7 (171 mg, 79%) as a yellow solid. .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 8.78 (d, J=9.2 Hz, 2H), 8.45-8.34 (m, 2H), 8.00 (d, J=8.2 Hz, 2H), 7.94-7.84 (m, 3H), 7.76 (t, J=7.1 Hz, 2H), 7.49 (d, J=7.3 Hz, 1H), 6.98 (s, 5H), 4.88 (s, 3H). .sup.11B NMR (128 MHz, DMSO-d.sub.6) δ-1.27. .sup.19F NMR (376 MHz, DMSO-d.sub.6) δ-148.35. .sup.13C NMR (101 MHz, DMSO-d.sub.6) δ 160.5, 141.4, 140.8, 139.3, 138.4, 131.6, 130.9, 130.8, 130.7, 129.6, 128.3, 128.1, 127.8, 127.4, 125.6, 119.3, 39.0.

##STR00023##

9-(2-Bromo-4-methylphenyl)-10-methylacridinium tetrafluoroborate (OPC8)

[0103] Following the general procedure using 2-bromo-4-methylbenzenediazonium tetrafluoroborate (142 mg, 0.5 mmol), the residue was purified by flash chromatography on silica gel to afford the desired compound OPC8 (126 mg, 56%) as a yellow solid. .sup.1H NMR (400 MHz, Methylene Chloride-d.sub.2) δ 8.66 (d, J=9.2 Hz, 2H), 8.50-8.35 (m, 2H), 7.99-7.75 (m, 5H), 7.51 (d, J=7.5 Hz, 1H), 7.29 (d, J=7.8 Hz, 1H), 4.98 (s, 3H), 2.57 (s, 3H). .sup.11B NMR (128 MHz, Methylene Chloride-d.sub.2) δ-1.13. .sup.13C NMR (101 MHz, Methylene Chloride-d.sub.2) δ 160.4, 143.1, 141.5, 139.3, 133.8, 130.8, 130.7, 129.8, 128.8, 128.2, 125.9, 121.8, 118.4, 38.9, 20.8 .sup.19F NMR (376 MHz, Methylene Chloride-d.sub.2) δ-152.94. HRMS (ESI) (m/z): [M].sup.+ calcd. For C.sub.21H.sub.17N.sup.79Br: 362.0539, found: 362.0542.

Example 2: Screening of Acridinium-Based Photoredox Catalysts in Oxidation of β-O-4 Lignin's Model to Aromatics

[0104] To test the performance of the modular acridinium catalysts, 2-(2-methoxyphenoxy)-1-phenylethanol (1) was selected as a simple nonphenolic β-O-4-type model substrate owing to this linkage is the most abundant in native Lignin (45-60%). The acridinium-based photoredox catalysts (OPC1 to 8) from example 1 were tested. Results are summarized in Table 2 below.

[0105] The reaction was carried out in the presence of 0.75 mol % of OPC in DMSO/MeOH/water as solvent mixtures in 8:8:1 mixing ratio under atmospheric pressure of O.sub.2 and blue LEDs irradiation for 12 h (further tests have shown the reaction can also be done under atmospheric pressure of air and blue LEDs irradiation for 12 h). We firstly examined the catalytic activity of commercially available Fukuzumi's catalyst, but a moderate conversion of 1 was observed with the formation of oxidized product 2 in only 5% (Table 2, entry 1).

[0106] Surprisingly, 1-phenylethane-1,2-diol (3) resulting from the C—O bond breakage was the major product, albeit in a very poor yield. This highlights the fact that acridiniums can be an effective OPC for oxidative C—O bond cleavage of the lignin's models using oxygen associated with visible-light as sustainable oxidant systems, all encouraging us to screen other acridinium-based structures to obtain higher yield in favor of 3. 9-Phenyl-10-methylacridium, bromo, ester, and acetyl, para-substituted 9-phenyl-10-methylacridiums give a similar trend of reactivity (Table 2, entries 2-5).

[0107] Interestingly, 10-methylacridium substituted by an ortho-substituted aryl group at C9-position give higher conversion. When the reaction is carried out with the photocatalyst OPC5 with a 2-bromophenyl at the C9 position, the C—O bond cleavage occurred in high yield affording 3 in 84% isolated yield without the formation of overoxidized products 4 and 5 (Table 2, entry 6). The catalyst OPC6 and OPC7 with 2-iodophenyl and 2-biphenyl C9-substituent, respectively, gives a slightly lower yield in 3, suggesting that 2-bromophenyl is the best design for this transformation (Table 2, entries 7 and 8). The OPC8 bearing a 2-bromo and 4-methyl substituents on the C9aryl also displayed a good reactivity affording 3 in 78% yield (Table 2, entry 9).

##STR00024##

TABLE-US-00002 TABLE 2 Fukuzumi and OPCs oxidation of β-O-4 lignin's model 1 results Yield Yield Yield Yield Conversion in in in in Entry OPC (%) 2 (%) 3 (%) 4 (%) 5 (%) 1 Fukuzumi 20 5 10 trace 8 (CAS 1442433-71-7) 2 OPC1 35 8 15 <5 9 3 OPC2 28 9 12 <5 <5 4 OPC3 30 <5 12 <5 12 5 OPC4 31 <5 15 7 11 6 OPC5 100 0 89 (84) 0 0 7 OPC6 61 — 52 0 0 8 OPC7 82 — 58 10 12 9 OPC8 100 21 78 0 0 The conversion is based on 1 consumption, and the yields are determined by CG-analysis using biphenyl as the internal standard. Isolated yield is shown in parentheses

[0108] Compounds according to the invention all gave better conversion percentage than the Fukuzumi catalyst. They all represent a better alternative to lignin depolymerisation.

[0109] The reaction is also simple to carry out and can be done under 02 or air atmosphere.

Example 3: Scope of β-O-4 Lignin's Model Substrates in Photocatalytic C—O Bond Cleavage

General Procedure for the in Photocatalytic C—O Bond Cleavage:

[0110] To a 25 mL Schlenk tube was added Lignin model (0.5 mmol), 9-(2-Bromophenyl)-10-methylacridin-10-ium tetrafluoroborate OPC5 (1.6 mg, 0.00375 mmol, 0.75 mol %,), DMSO (2.3 mL), MeOH (2.3 mL) and water (0.4 mL) were successfully added. After purging the flask three times with vacuum and two times with argon, 02 atmosphere was incorporated through an 02-filled balloon (further tests have shown the reaction can also be done under air atmosphere incorporated through open air). The Schlenk was positioned on a stir plate approximately 2-3 cm from two ABI PAR38 (24′A LED lamp supplying blue light (λ=440-460 nm). Fans were used for cooling. After 12 hours irradiation, the reaction was quenched by addition of 20 ml CH.sub.2Cl.sub.2 and the crude mixture was washed with 3 mL water 3 times, then solvent was removed under reduced pressure and purified by flash column chromatography on silica gel to give the pure product.

[0111] A variety of lignin model systems were subjected to the photooxidative catalytic OPC5 to probe the scope (Scheme 2). Results are summarized in table 3.

[0112] Firstly, the methoxy substitution pattern of the phenolic part on the simplified β-O-4 model systems was varied. From 2-(3,5-dimethoxyphenoxy)-1-phenylethanol (6) and 2-(3,4-dimethoxyphenoxy)-1-phenylethanol (7), the optimized conditions lead to the selective C—O bond cleavage affording the 1-phenylethane-1,2-diol (2) in 71% and 75% yield, respectively. These results further prompted the examination of other β-O-4 model systems 8-10, which are good representations of the different units present in native lignin (coumaryl, coniferyl, and sinapyl alcohols). Using 2-(2-methoxyphenoxy)-1-(4-methoxyphenyl)ethan-1-ol (8) in which both arene rings display similar electronic properties the photocatalytic C—O bond cleavage affords the 1-(4-methoxyphenyl)ethane-1,2-diol (14) in only 45% yield. However, when the phenolic part contains two methoxy groups such as in 9 or 10, the diol 14 was isolated in better yields. Again, the C—O bond cleavage of 11, in which both rings have methoxy substituent, occurred to afford 16 in 46% yield, while 16 is obtained in better yield when the phenol part contains two methoxy group whatever its substitution pattern 3,5 or 3,4 (from 12 and 13).

1-Phenylethane-1,2-diol (2): .SUP.1.H NMR (400 MHz, CDCl.SUB.3.) δ 7.37-7.30 (m, 5H), 4.81-4.79 (m, 1H), 3.74-3.71 (m, 1H), 3.64-3.62 (m, 1H), 2.92 (s, 2H). .SUP.13.C NMR (100 MHz, CDCl.SUB.3.) δ 140.4, 128.5, 128.0, 126.1, 74.7, 68.1

1-(4-Methoxyphenyl)ethane-1,2-diol (14): .SUP.1.H NMR (400 MHz, CDCl.SUB.3.) δ 7.23 (2H, d, J=6.6 Hz), 6.86 (2H, d, J=6.6 Hz), 4.71 (1H, d, J=8.0 Hz), 3.78 (3H, s), 3.69-3.54 (2H, m), 3.46 (1H, s), 3.11 (1H, s). .SUP.13.C NMR (100 MHz, CDCl.SUB.3.) δ 159.4, 132.7, 127.4, 114.0, 77.4, 77.1, 76.9, 74.4, 68.1, 55.3

1-(3-Methoxyphenyl)ethane-1,2-diol (15): 1H NMR (400 MHz, CDCl.SUB.3.) δ=7.25 (t, J=7.8 Hz, 1H), 6.92 (d, J=9.0 Hz, 2H), 6.83 (d, J=8.4 Hz, 1H), 4.77 (dd, J=8.4, 4.8 Hz, 1H), 3.79 (s, 3H), 3.74-3.71 (m, 1H), 3.65-3.61 (m, 1H), 2.05 (br s, 2H). .SUP.13.C NMR (100 MHz, CDCl.SUB.3.) δ 159.9, 142.4, 129.7, 118.5, 113.5, 111.8, 74.7, 68.2, 55.4

[0113] ##STR00025##

TABLE-US-00003 TABLE 3 Scope of β-O-4 Lignin's Model Substrates in Photocatalytic C—O Bond Cleavage Diols β-O-4 Lignin's Model Substrates Yield Entry Name R.sup.A R.sup.B R.sup.C R.sup.D R.sup.E R.sup.F Name (%) 1  6 H H H OMe H OMe  3 71 2  7 H H H OMe OMe H  3 75 3  8 OMe H OMe H H H 14 45 4  9 OMe H H OMe OMe H 14 78 5 10 OMe H H OMe H OMe 14 90 6 11 H OMe OMe H H H 15 46 7 12 H OMe H OMe OMe H 15 88 8 13 H OMe H OMe H OMe 15 86

[0114] In conclusion, a novel approach toward the valorisation of lignin and related systems has been developed by designing a novel organic photoredox catalyst. Various lignin model compounds underwent a smooth transformation to afford the corresponding C—O bond cleavage product in moderate to excellent yields under mild reaction conditions using oxygen and visible-light as oxidant. The unique photoredox properties of this acridinium-based catalysts according to the invention have allowed the selective formation of 1-arylethane-1,2-diols in high yields that constitutes a vital step toward converting lignin to value-added, low-molecular-weight aromatics.

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