Electrochemical synthesis of new catechol derivatives

Electrochemical oxidation of catechols (1a-e) has been studied in the presence of 2-acetylcyclopentanone (3) as a nucleophile in aqueous solutions, using cyclic voltammetry and controlled-potential coulometry. The results indicate that the quinones derived from catechols (1a-e), participate in Michael addition reactions with anion of 2-acetylcyclopentanone (3) and via EC mechanism pathway, converted to corresponding catechol derivatives (4a-e). In this work, we derived novel catechol derivatives with good yields based on electrochemical oxidation in aqueous solutions, at carbon electrode in an undivided cell, using environmentally friendly method.     

A new facile electrochemical method for the synthesis of 4-(pyridine-2-ylthio)benzene-l,2-diols

Electrochemical oxidation of catechols (1a-1c) has been studied in the presence of 2-mercaptopyridine (3) as a nucleophile in water solution using cyclic voltammetry and controlled-potential coulometry. The results revealed that the quinones derived from catechols (1a-1c) participate in Michael addition reaction with 2-mercaptopyridine (3) and converted to the corresponding (pyridine-2-ylthio)benzene-l,2-diol derivatives (4a-4c), via an EC mechanistic pathway. The electrochemical synthesis of compounds 4a-4c has been successfully performed at a carbon rod electrode and in an undivided cell with good yields and high purity.     

Mechanistic study of electrochemical oxidation of catechols in the presence of 4-hydroxy-1-methyl-2(1H)-quinolone: Application to the electrochemical synthesis

Electrochemical oxidation of catechols (1a-1c) has been studied in the presence of 4-hydroxy-1-methyl-2(1H)-quinolone (3) as a nucleophile in aqueous solution using cyclic voltammetry and controlled-potential coulometry. The results indicate that the quinones derived from catechols (1a-1c) participate in Michael addition reactions with 3 to form the corresponding benzofuran (or isochromeno[4,3-c]quinoline) derivatives (6a-6c). The electrochemical synthesis of (6a-6c) has been successfully performed in an undivided cell in good yield and purity. The oxidation mechanism was deduced from voltammetric data and by coulometry at controlled-potential. The products have been characterized after purification by IR, ¹H NMR, ¹³C NMR and MS.     

A facile galvanostatic method for the synthesis of quinoxalinediones

Electrochemical oxidation of catechols (1a-d) has been studied in the presence of N,N-dimethylethylendiamine (3) as a nucleophile in aqueous solutions, using cyclic voltammetry, constant-current coulometry and controlled-potential coulometry. The results indicate that the quinones derived from catechols (2a-d) participate in Michael addition reactions with N,N′-dimethylethylendiamine (3) via the ECECE mechanism to form the corresponding quinoxalinedione derivatives (6a-c).     

Electrooxidation of 4-methylcatechol in the presence of barbituric acid derivatives

Electrooxidation of 4-methylcatechol (1) in the presence of 1,3-dimethylbarbituric acid (2a) and 1,3-diethylthiobarbituric acid (2b) as nucleophiles has been studied in detail by cyclic voltammetry and controlled-potential coulometry. The results indicate that 1 can be oxidized to its related o-benzoquinone (1a) and without conversion to its quinone methide tautomeric form, via an ECEC mechanism pathway, is converted to barbiturate derivatives (5a-b). The electrochemical synthesis of 5a-b have been successfully performed in one-pot in an undivided cell.     

Effects of internal linkage groups of fluorinated diamine on the optical and dielectric properties of polyimide thin films

To investigate the difference of the trifluoromethyl (CF₃) group and ether group affecting the optical property of fluorinated polyimides (PIs), we prepared 4,4′-bis(4-amino-2-trifluoromethylphenoxy)diphenyl ether (4) with three ether groups and 2,2-bis[4-(4-amino-2-trifluoromethylphenoxy)phenyl]hexafluoropropane (5) with four CF₃ groups with 2-chloro-5-nitrobenzotrifluoride and 4,4′-dihydroxydiphenyl ether or 2,2-bis(4-hydroxyphenol)hexafluoropropane. Two series of organosoluble and light-colored PIs (4a-4c, 5a-5c) were synthesized from 4 and 5 with various aromatic dianhydrides: 3,3,4,4-benzophenonetetracarboxylic dianhydride (BTDA) (a), 4,4-oxydiphthalic anhydride (ODPA) (b), and 4,4-hexafluoroisopropylidenediphthalic anhydride (6FDA) (c), prepared through a typical two-step polymerization method. These PIs were soluble in amide polar solvents and even in less polar solvents. The glass-transition temperatures (T_g) of 4a-5c were 221-249 °C and the 10% weight-loss temperatures were above 530 °C. Their films had cutoff wavelengths between 339 and 399 nm and yellowness index ranges from 1.95 to 42.60. The dielectric constants estimated from the average refractive indices are 2.59-2.93 (1 MHz). In a comparison of the PI series based on 4, 5, and 4,4′-bis(4-amino-2-trifluoromethylphenoxy)biphenyl (6), we found that the CF₃ group and ether group on the diamine had almost same effect in lowering the color, but the ether group had better thermal stability. The color intensity of the three PI series was lowered in the following order: 6 > 4 > 5. The PI 5c, synthesized from diamine 5 and dianhydride c, had six CF₃ groups in a repeated segment and ether group at the same time, so it exhibited the lightest color among the three series.     

Mechanistic study of electrochemical oxidation of o-dihydroxybenzenes in the presence of 4-hydroxy-1-methyl-2(1H)-quinolone: Application to the electrochemical synthesis

Electrochemical oxidation of o-dihydroxybenzenes (1a and 1b) has been studied in the presence of 4-hydroxy-1-methyl-2(1H)-quinolone (3) as a nucleophile in aqueous solution using cyclic voltammetry and controlled-potential coulometry. The results indicate that the o-quinones derived from o-dihydroxybenzenes (1a and 1b) participate in 1,4-(michael) addition reactions with 3 to form the corresponding new o-dihydroxybenzene derivatives (6a and 6b). We propose a mechanism for the electrode process. The efficient electrochemical synthesis of 6a and 6b has been successfully performed at carbon rod electrodes in an undivided cell in good yield and purity. The products have been characterized after purification by IR, ¹H NMR, ¹³C NMR and MS.     

Synthesis and gas permeation properties of various Si-containing poly(diarylacetylene)s and their desilylated membranes

Diarylacetylene monomers having trimethylsilyl groups and other substituents (substituted biphenyl, 1a and 1b; trimethylsilylmethylphenyl, 1c-e) were synthesized and polymerized with TaCl₅-n-Bu₄Sn catalyst to produce the corresponding poly(diarylacetylene)s (2a-d). Polymers 2a-c had high molecular weights and were soluble in common organic solvents. Free-standing membranes of 2a-c as well as previously reported 2f-h were prepared by the solution-casting method. Desilylation of these Si-containing polymer membranes was carried out with trifluoroacetic acid to afford 3a, 3b, and 3f-h. Upon desilylation, biphenyl-containing membranes became less permeable (3a, b), whereas fluorene-containing membranes became more permeable (3f-h). In particular, 3h exhibited extremely high gas permeability (PO₂ = 9800 barrers), which is about the same as that of poly(1-trimethylsilyl-1-propyne). Desilylated membranes 3a and 3f-h showed different gas permeability from that of polymers 2i-k which have the identical chemical structures and obtained directly by the polymerization of the corresponding monomers.     

Paired electrochemical synthesis of new organosulfone derivatives

Electrochemical oxidation of “cathodically generated 4-aminocatechol (2)” has been studied in the presence of 4-toluenesulfinic acid (4a) and benzenesulfinic acid (4b) as nucleophiles in aqueous solutions, using cyclic voltammetry and controlled-potential coulometry. The results indicate that the o-benzoquinone derived from 4-aminocatechol (2) participates in Michael addition reaction with 4a or 4b to form the corresponding new organosulfone derivatives (5a and 5b). In this work we have proposed a mechanism for the electrode process. A Fe(CN)₆³⁻/Fe(CN)₆⁴⁻ redox mediator was used for the anodic oxidation of 4-aminocatechol (2) to the corresponding o-quinone 3. The indirect electrochemical process consists of a multi-step such as (a) cathodic reduction of 4-nitrocatechol (1) to 4-aminocatechol (2), (b) chemical oxidation of 4-aminocatechol (2) to 4-aminoquinone (3) with the resulting Fe(CN)₆³⁻, (c) the chemical reaction of 4-aminoquinone (3) with 4-toluenesulfinic acid (4a) or benzenesulfinic acid (4b), and (d) the anodic regeneration of Fe(CN)₆³⁻. The paired electrochemical synthesis of organosulfone derivatives (5a and 5b) has been successfully performed in an one-pot process at carbon rod electrode as a working and platinum as a counter electrode in an undivided cell.     

Electrochemical characterisation of tetra- and octa-substituted oxo(phthalocyaninato)titanium(IV) complexes

The synthesis and electrochemical characterisation of the following oxotitanium tetra-substituted phthalocyanines are reported: 1,(4)-(tetrabenzyloxyphthalocyaninato)titanium(IV) oxide (5a); 1,(4)-{tetrakis[4-(benzyloxy)phenoxy]phthalocyaninato}titanium(IV) oxide (5b); 2,(3)-(tetrabenzyloxyphthalocyaninato)titanium(IV) oxide (6a) and 2,(3)-{tetrakis[4-(benzyloxy)phenoxy]phthalocyaninato}titanium(IV) oxide (6b). The electrochemical characterisation of complexes octa-substituted with 4-(benzyloxy)phenoxy (9b), phenoxy (9c) and tert-butylphenoxy (9d) groups is also reported. The cyclic voltammograms of the complexes exhibit reversible couples I-III and couple IV is quasi-reversible for complexes 5a, 5b, 6a and 6b. The first two reductions are metal-based processes, confirmed by spectroelectrochemistry to be due to Ti^IVPc²⁻/Ti^IIIPc²⁻ and Ti^IIIPc²⁻/Ti^IIPc²⁻ redox processes and the last two reductions are ring-based processes due to Ti^IIPc²⁻/Ti^IIPc³⁻ and Ti^IIPc³⁻/Ti^IIPc⁴⁻. Chronocoulometry confirmed a one-electron transfer at each reduction step. The electrochemistry of the above complexes is also compared to the previously reported 5c, 5d, 6c and 6d.     

Synthesis of 6-(4-diethylamino)phenyl-2-oxo-2H-pyran-3-carbonitorile derivatives and their fluorescence in solid state and in solutions

One-pot synthesis of a new 2-pyrone dye (3a) by the reaction of 4-diethylamino-acetophenone (1) with methyl 2-cyano-3,3-bis(methylsulfanyl)acrylate (2) in the presence of sodium hydroxide as the base was carried out in DMSO. Compound 4a was synthesized by the replacement of methylsulfanyl group of 3a with dimethylamine at 4-position of pyrone ring. Similarly, compound 5a was prepared via the reaction of 3a with diethyl malonate. Compounds 3a-5a exhibited the following fluorescence in the solid state: red (3a), green (4a), and orange (5a). In addition, it was revealed that 2-pyrone dyes exhibit fluorescence in various solvents and show positive solvatochromism. Compounds 3a and 5a exhibited intense fluorescence in chloroform and dichloromethane (fluorescence quantum yield Φ: 0.94-0.95). In contrast, compound 4a exhibited intense fluorescence in polar solvents (methanol: Φ = 0.92). These 2-pyrone dyes have the potential for applications in various fields.     

Synthesis of poly(1-β-naphthyl-2-phenylacetylene) membranes through desilylation and their properties

The polymerization of 1-β-naphthyl-2-[(p-trimethylsilyl)phenyl]acetylene (8a) with TaCl₅-n-Bu₄Sn in cyclohexane provided a high molecular weight polymer (9a) (M_w=3.4×10⁶). The corresponding monomers having p-dimethyl-t-butylsilyl and p-dimethyl(10-pinanyl)silyl groups in place of p-trimethylsilyl group in 8a also polymerized in a similar way to give high molecular weight polymers (9b, 9c, respectively; M_w>1×10⁶). All these polymers were soluble in many common solvents such as toluene and chloroform, and provided free-standing membranes by casting from toluene solution. The oxygen permeability coefficients (P_O2) of 9a at 25 °C was as high as 3500 barrers. The membrane of poly(1-β-naphthyl-2-phenylacetylene) (10a) was prepared by desilylation of the membrane of 9a with trifluoroacetic acid. Polymer 10a was insoluble in any solvents, and showed high thermal stability (the onset temperature of weight loss in air ∼470 °C). The P_O2 value of 10a reached 4300 barrers. Not only the membrane of 9c but also its desilylation product 10c exhibited large optical rotations ([α]_D=+2924 and +9800°, respectively) and strong CD signals. This indicates that the membrane of 10c maintains the helical main chain conformation of 9c with a large excess one-handed helix sense.     

Electrochemical study of stable N-alkoxyarylaminyl radicals

The electrochemical study of N-tert-butoxy-2,4-diphenyl-6-tert-butylphenylaminyl (1a), N-tert-butoxy-2,4-bis(4-chlorophenyl)-6-tert-butylphenylaminyl (1b), N-[2-(methoxycarbonyl)-2-propyl]-2,4-diphenyl-6-tert-butylphenylaminyl (2), and N-tert-butoxy-2,4,6-tris(4-chlorophenyl)phenylaminyl radicals (3) was performed by cyclic voltammetry using acetonitrile as the solvent and Bu₄NPF₆ as the supporting electrolyte. On cathodic scan (100 mV/s), all the radicals gave chemically reversible cyclic voltammograms, and the were determined to be −1.405 V (1a), −1.310 V (2a), −1.282 V (2b), and −1.195 V (3) (versus Fc⁺/Fc), respectively. On anodic scan (100 mV/s), on the other hand, 1a, 1b and 2 showed chemically reversible cyclic voltammograms, but 3 exhibited a partially reversible couple even on a scan rate of 500 mV/s, indicating that the cation species of 3 was less stable. The determined for 1a, 1b, 2 and 3 were 0.220, 0.280, 0.318 and 0.294 V (versus Fc⁺/Fc), respectively. The electrochemical data were compared with those of thioaminyl radicals, the corresponding sulfur analogues of 1-3.     

Novel poly(diphenylacetylene)s with both alkyl and silyl groups as gas permeable membranes: Synthesis, desilylation, and gas permeability

Diphenylacetylenes having a dimethyloctylsilyl group and an alkyl group at para positions [Me₂n-C₈H₁₇SiC₆H₄CCC₆H₄R; R = H (1a), i-Pr (1b), t-Bu (1c), n-Bu (1d)] and having only an alkyl group [PhCCC₆H₄R; R = i-Pr (1B), t-Bu (1C)] were synthesized and then polymerized with TaCl₅/n-Bu₄Sn catalyst to provide the corresponding poly(diphenylacetylene)s (2a, 2b, 2c, 2d, 2B, and 2C). The formed polymers afforded tough free-standing membranes by casting from toluene solutions. Desilylation reaction of Si-containing membranes (2a-d) was carried out with trifluoroacetic acid to give the desilylated membranes (3a-d). The permeability of these membranes to O₂, N₂, and CO₂ were determined. All the Si-containing membranes exhibited almost the same gas permeability. The desilylation of Si-containing membranes of 2a-c resulted in large increase of gas permeability. No apparent increasing of gas permeability was observed in the desilylation of 2d. To clarify the effects of desilylation, CO₂ diffusivity (D(CO₂)), CO₂ solubility (S(CO₂)), and fractional free volume (FFV) of the polymer membranes were investigated. The S(CO₂) values of desilylated membranes were much larger than that of Si-containing counterparts. The D(CO₂) and FFV of membranes of 2a-c increased through desilylation. The desilylated membrane of 3d had small D(CO₂) value and almost the same FFV compared with 2d. Further, the comparison of the permeability between three types of membranes with the same chemical structure revealed that the microvoids were not generated by the desilylation of membranes of poly(diphenylacetylene)s containing alkyl groups.     

Synthesis and properties of ornithine- and lysine-based poly(N-propargylamides). Responsiveness of the helical structure to acids

Ornithine- and lysine-based novel N-propargylamides, N-α-tert-butoxycarbonyl-N-δ-fluorenylmethoxycarbonyl-l-ornithine-N′-propargylamide (1), N-α-tert-butoxycarbonyl-N-?-fluorenylmethoxycarbonyl-l-lysine-N′-propargylamide (2), N-α-fluorenylmethoxycarbonyl-N-δ-tert-butoxycarbonyl-l-ornithine-N′-propargylamide (3), and N-α-fluorenylmethoxycarbonyl-N-?-tert-butoxycarbonyl-l-lysine-N′-propargylamide (4) were synthesized and polymerized with a rhodium catalyst. Polymers with moderate molecular weights were obtained in good yields. Poly(1)-poly(4) showed strong Cotton effects in THF, whose sign and wavelength depended on the substituents. They were satisfactorily converted into the corresponding polymers [poly(1a)-poly(4a)] with free amino groups. Poly(1a) and poly(2a) also formed a helix, while poly(3a) and poly(4a) did not. Poly(1a) and poly(2a) decreased the CD intensity by the addition of m- and o-phthalic acids.     

Tyrosine-based poly(m-phenyleneethynylene-p-phenyleneethynylene)s. Helix folding and responsiveness to a base

The Sonogashira-Hagihara polymerization of 3′,5′-diiodo-N-α-tert-butoxycarbonyl-l-tyrosine methyl ester (1) and 3′,5′-diiodo-N-α-tert-butoxycarbonyl-O-methyl-l-tyrosine methyl ester (2) with para-diethynylbenzene (3) was carried out to obtain optically active poly(m-phenyleneethynylene-p-phenyleneethynylene)s [poly(1) and poly(2)] with M_n’s ranging from 9900 to 15,000 in 80-87% yields. Poly(1) exhibited intense CD signals in DMSO and THF, but did not in CH₂Cl₂, indicating that it took a predominantly one-handed helical conformation in the former two solvents. On the other hand, there was no evidence for poly(2) to take a helical structure in these solvents. Poly(1) turned the CD sign at 390 nm from plus to minus in DMSO/H₂O = 9/1 (v/v) by the addition of NaOH. Alkaline hydrolysis of ester moieties of poly(1) and poly(2) gave the corresponding polymers having carboxy groups [poly(1a) and poly(2a)]. Poly(1a) and poly(2a) increased the CD intensity by the addition of NaOH.     

Performance improvement of polybenzoxazine by alloying with polyimide: effect of preparation method on the properties

Polymer alloys of polyimide and polybenzoxazine were prepared from the combination of a bifunctional benzoxazine monomer, 6,6′-(1-methylethylidene)bis(3,4-dihydro-3-2H-1,3-benzoxazine) (B-a) and a soluble polyimide (PI) or its precursor, poly(amide acid) (PAA), that was synthesized from oxydianiline (ODA) and bisphenol A di(phthalic anhydride) ether (BPADA). It was observed from DSC that the onset temperature for the curing exotherm of B-a in the blend with PAA was remarkably lowered compared with that of pristine B-a, while the curing temperature of B-a in the blend with PI was almost the same as that of pristine B-a. The cast films of PI/B-a or PAA/B-a were thermally treated at 150, 200 and 240 °C for 2 h each, affording deep wine, transparent films. The PI component in the polymer alloy films from PI/B-a dissolved thoroughly. On the other hand, the polymer alloy films from PAA/B-a were not soluble at all in NMP. The polymer alloy films from both PI/B-a and PAA/B-a showed only one glass transition temperature (T_g) from their viscoelastic analyses. The T_g values remarkably increased as the content of PI increased. The thermal stabilities of both films from PI/B-a and PAA/B-a increased as the PI component increased in the similar manner.     

Synthesis and electrochemical characterisation of benzylmercapto and dodecylmercapto tetra substituted cobalt, iron, and zinc phthalocyanines complexes

The work reports on cyclic voltammetry (CV), square wave voltammetry and spectroelectrochemistry of the following complexes: tetrakis (benzylmercapto) phthalocyanine complexes of Zn(II) (ZnTBMPc, 4a), Co(II) (CoTBMPc, 5a), and Fe(II) (FeTBMPc 6a); tetrakis (dodecylmercapto) phthalocyanine complexes of Zn(II) (ZnTDMPc, 4b), Co(II) (CoTDMPc, 5b), and Fe(II) (FeTDMPc, 6b). More reversible CV couples were observed for complexes 4a, 5a, and 6a containing thiol phenyl ring substituents. Complexes 4b, 5b, and 6b containing long chain thiol substituents showed less reversible couples. Complexes 6a and 6b showed a relatively large number of redox processes (5 for 6a and 6 for 6b) within the potential window employed in this work. The processes for FePc derivatives (6a) are assigned to Fe^IIIPc⁻¹/Fe^IIIPc⁻², Fe^IIIPc⁻²/Fe^IIPc⁻², Fe^IIPc⁻²/Fe^IPc⁻², Fe^IPc⁻²/Fe^IPc⁻³, and Fe^IPc⁻³/Fe^IPc⁻⁴ and for the CoPc derivative (5a) to Co^IIIPc⁻¹/Co^IIIPc⁻², Co^IIIPc⁻²/Co^IIPc⁻², Co^IIPc⁻²/Co^IPc⁻², and Co^IPc⁻²/Co^IPc⁻³.