Sulfur Analogues Research Articles

Effect of Chalcogen Atom on the Properties of Naphthobischalcogenadiazole-Based π-Conjugated Polymers

We here discuss the effect of chalcogen atom on the properties of π-conjugated polymers based on electron deficient fused π-electron systems, naphtho[1,2-c:5,6-c′]bis[1,2,5]oxadiazole (NOz), naphtho[1,2-c:5,6-c′]bis[1,2,5]thiadiazole (NTz), and naphtho[1,2-c:5,6-c′]bis[1,2,5]selenadiazole (NSz). We synthesize new donor–acceptor polymers having NOz and NSz combined with a quaterthiophene donor unit, namely, PNOz4T and PNSz4T, respectively. Physicochemical properties, structures, and charge transport properties of PNOz4T and PNSz4T in comparison with the sulfur analogue (PNTz4T) are discussed. As both NOz and NSz have a higher electron deficient nature than NTz, PNOz4T and PNSz4T are found to possess deeper frontier orbital energy levels. In particular, PNOz4T have a sufficiently deep lowest unoccupied molecular orbital (LUMO) energy level which allows for ambient ambipolar behavior in transistor devices. Interestingly, whereas PNSz4T is mostly amorphous in the thin film, PNOz4T forms a highly crystalline s...

One-pot, solvent-free synthesis via Biginelli reaction: Catalyst-free and new recyclable catalysts

AbstractFree catalyst one-pot three components coupling of aldehydes, β-dicarbonyl compounds, and urea was performed to afford both the corresponding 3,4-dihydropyrimidine-2-ones (DHPOs, (1–9)a) and their sulfur analogs 3,4-dihydropyrimidine-2-thiones (DHPTs, (1–9)b), synthesized in the presence of uranyl acetate (UA) and succinimide sulfonic acid (SuSA) as catalysts under the same conditions via Biginelli condensation protocol. Interestingly, the free catalyst reactions were performed for 4 h for DHPOs with the yields of high to excellent, while in the cases of DHPTs, the yield was lower. But when the UA or SuSA was used, the yields (both of DHPOs and DHPTs) were high to excellent and the reaction times were either 2.5 or 1 h, respectively. Also, these two catalysts were recyclable for four consecutive runs.

On the Role of Chalcogen Donor Atoms in Diimine‐Dichalcogenolate PtII SONLO Chromophores: Is It Worth Replacing Sulfur with Selenium?

AbstractTwo new diimine‐diselenolate PtII chromophores [Pt(bipy)(Me‐dset)] (1) and [Pt(phen)(Me‐dset)] (2) (Me‐dset2– = N‐methyl‐2‐thioxothiazoline‐4,5‐diselenolate) were synthesized and characterized. The effect of replacing sulfur with selenium was investigated by comparing the UV/Vis spectroscopic and electrochemical properties of 1 and 2 with those of the corresponding sulfur analogues, [Pt(bipy)(Me‐dmet)] (3) and [Pt(phen)(Me‐dmet)] (4), with a particular focus on their linear and nonlinear optical properties.

OP45 - Sulphur and selenium species as targets and protective species in inflammatory diseases: Why speed matters: understanding key mechanisms of protein modification

Activated leukocytes generate multiple oxidants to kill invading pathogens including O 2 -• , H 2 O 2 , NO • , peroxynitrous acid (ONOOH) and hypohalous acids (HOCl, HOBr, HOSCN) via the activity of NADPH oxidases, nitric oxide synthases (e.g. iNOS) and myeloperoxidase (MPO). Inappropriate generation can however result in tissue damage, with this associated with multiple human inflammatory pathologies (e.g. cardiovascular disease, some cancers, rheumatoid arthritis, asthma, cystic fibrosis, neurodegenerative conditions). Sulphur residues in peptides and proteins are key targets. Competition kinetic methods have yielded rate constants, k, for reaction of HOCl with Cys and GSH of 3.6 x 10 8 and 1.2x10 8 M- 1 s- 1 , respectively. These values are ~10-fold higher than reported previously, and are some of the fastest reactions of non-radical oxidants, emphasizing the key role of thiols in protection. N-Ac-methionine also reacts very rapidly (k 1.7x10 8 M- 1 s- 1 ). ONOOH reacts rapidly with Cys and Met with k ~ 2x10 3 and 2x10 2 M- 1 s- 1 respectively. Selenium compounds should react faster than the sulphur analogues. Seleno-compounds, including novel seleno sugars react with HOCl with k ~10 8 M- 1 s- 1 and ~ 100-fold faster than the sulphur analogues. A similar rate enhancement is seen with ONOOH, with k for ONOOH and selenocysteine ~2x10 5 M- 1 s- 1 . The selenoxides formed on oxidation of these species, can be readily reduced by thiols (e.g. GSH) and some enzyme systems, making these catalytic protective agents. The seleno-sugars decrease oxidant-mediated damage to isolated proteins and human plasma at low concentrations. Examination of these seleno sugars in an animal model of wound healing has shown that topical application markedly enhances wound closure in both normal and diabetic animals. These studies demonstrate that novel selenium-containing molecules may be potent modulators of damage at sites of acute and chronic inflammation, and be beneficial in multiple human pathologies.

Mechanistic and Kinetic Studies on the Homogeneous Gas-Phase Formation of PCTA/DTs from 2,4-Dichlorothiophenol and 2,4,6-Trichlorothiophenol

Polychlorinated thianthrene/dibenzothiophenes (PCTA/DTs) are sulfur analogues compounds to polychlorinated dibenzo-p-dioxin/dibenzofurans (PCDD/Fs). Chlorothiophenols (CTPs) are key precursors to form PCTA/DTs. 2,4-DCTP has the minimum number of Cl atoms to form 2,4,6,8-tetrachlorinated dibenzothiophenes (2,4,6,8-TeCDT), which is the most important and widely detected of the PCDTs. In this paper, quantum chemical calculations were carried out to investigate the homogeneous gas-phase formation of PCTA/DTs from 2,4-DCTP and 2,4,6-TCTP precursors at the MPWB1K/6-311+G(3df,2p)//MPWB1K/6-31+G(d,p) level. Several energetically feasible pathways were revealed to compare the formation potential of PCTA/DT products. The rate constants of the crucial elementary reactions were evaluated by the canonical variational transition-state (CVT) theory with the small curvature tunneling (SCT) correction over a wide temperature range of 600–1200 K. This study shows that pathways that ended with elimination of Cl step were dominant over pathways ended with elimination of the H step. The water molecule has a negative catalytic effect on the H-shift step and hinders the formation of PCDTs from 2,4-DCTP. This study, together with works already published from our group, clearly illustrates an increased propensity for the dioxin formation from CTPs over the analogous CPs.

Sulfur- and acyl chain-dependent influence of 2-methoxy-lysophosphatidylcholine analogues on β pancreatic cells.

Nutrient-induced increase in intracellular Ca(2+) concentration ([Ca(2+)]i) is one of the key mechanisms responsible for insulin release from pancreatic islet β cells. Lysophosphatidylcholine (LPC) was demonstrated to induce insulin secretion from β cells, activate glucose uptake and effectively lower blood glucose levels in mouse models of type 1 and 2 diabetes mellitus. The article hereby presents the results of a characterization of 2-OMe-LPC sulfur analogues with defined acyl residues in terms of their effect on intracellular Ca(2+) concentration and cellular membrane integrity in the murine βTC-3 cell model. Active LPC series that could induce calcium flux in βTC-3 cell model include unmodified LPC 12:0, 14:0, 16:0, and 18:0 as well as phosphorothioate analogues of LPC 12:0, 14:0 and 16:0. However, in the case of species bearing mirystoyl and palmitoyl residues [Ca(2+)]i was associated with membrane permeabilization as demonstrated by propidium iodide incorporation and lactate dehydrogenase release. LPC 12:0 (both unmodified and a sulfurcontaining counterpart) and unmodified LPC 18:0 did not demonstrate membrane disruption but acted as calcium inducers. Interestingly, no stimulation of calcium flux or membrane disruption was observed in the case of LPC analogues with two sulfur atoms introduced into a phosphate group. Experiments with nitrendipine and NiCl2 blocking voltage-dependent calcium channels and the general calcium influx, respectively, revealed remarkably that the compounds studied were involved in different signaling mechanisms while administered to the cell culture, which is clearly related to their chemical structure, both acyl chain and modification dependently.

Photoelectron Spectroscopy and Ionic Fragmentation of OSeCl2 and Its Analogue OSCl2 under VUV Irradiation.

The electronic structure and the dissociative ionization of selenium oxychloride, OSeCl2, have been investigated in the valence region by using results from both photoelectron spectroscopy (PES) and synchrotron-based photoelectron photoion coincidence (PEPICO) spectra. The PES is assigned with the help of quantum chemical calculations at the outer-valence Green's function (OVGF) and symmetry adapted cluster/configuration interaction (SAC-CI) levels. The first energy ionization is observed at 11.47 eV assigned to the ionization of electrons formally delocalized over the Se, Cl, and O lone pair orbitals. Irradiation of OSeCl2 with photons in the valence region leads to the formation of OSeCl2(•+), OSeCl(+), SeCl2(•+), SeCl(+), and SeO(•+) ions. Furthermore, the inner shell Se 3p, Cl 2p, and Se 3s electronic regions of OSeCl2 together with S 2p, Cl 2p, and S 2s electronic regions of thionyl chloride, OSCl2, have been studied by using tunable synchrotron radiation. Thus, total ion yield spectra and the fragmentation patterns deduced from PEPICO spectra at the various excitation energies have been studied. Cl(+), O(•+), and Se(•+) ions appear as the most intense fragments in the OSeCl2 PEPICO spectra, like in the sulfur analogue OSCl2, whose photofragmentation is dominated by the Cl(+), O(•+), and S(•+) ions. Fragmentation processes in OSCl2 leading to the formation of the double coincidences involving atomic ions appear as the most intense in the PEPIPICO spectra.

Bonding in Complexes of Bis(pentalene)dititanium, Ti2(C8H6)2.

Bonding in the bis(pentalene)dititanium “double-sandwich” species Ti2Pn2 (Pn = C8H6) and its interaction with other fragments have been investigated by density functional calculations and fragment analysis. Ti2Pn2 with C2v symmetry has two metal–metal bonds and a low-lying metal-based empty orbital, all three frontier orbitals having a1 symmetry. The latter may be regarded as being derived by symmetric combinations of the classic three frontier orbitals of two bent bis(cyclopentadienyl) metal fragments. Electrochemical studies on Ti2Pn†2 (Pn† = 1,4-{SiiPr3}2C8H4) revealed a one-electron oxidation, and the formally mixed-valence Ti(II)–Ti(III) cationic complex [Ti2Pn†2][B(C6F5)4] has been structurally characterized. Theory indicates an S = 1/2 ground-state electronic configuration for the latter, which was confirmed by EPR spectroscopy and SQUID magnetometry. Carbon dioxide binds symmetrically to Ti2Pn2, preserving the C2v symmetry, as does carbon disulfide. The dominant interaction in Ti2Pn2CO2 is σ donation into the LUMO of bent CO2, and donation from the O atoms to Ti2Pn2 is minimal, whereas in Ti2Pn2CS2 there is significant interaction with the S atoms. The bridging O atom in the mono(oxo) species Ti2Pn2O, however, employs all three O 2p orbitals in binding and competes strongly with Pn, leading to weaker binding of the carbocyclic ligand, and the sulfur analogue Ti2Pn2S behaves similarly. Ti2Pn2 is also capable of binding one, two, or three molecules of carbon monoxide. The bonding demands of a single CO molecule are incompatible with symmetric binding, and an asymmetric structure is found. The dicarbonyl adduct Ti2Pn2(CO)2 has Cs symmetry with the Ti2Pn2 unit acting as two MCp2 fragments. Synthetic studies showed that in the presence of excess CO the tricarbonyl complex Ti2Pn†2(CO)3 is formed, which optimizes to an asymmetric structure with one semibridging and two terminal CO ligands. Low-temperature 13C NMR spectroscopy revealed a rapid dynamic exchange between the two bound CO sites and free CO.

N‐Derivatives of peri‐Substituted Dichalcogenide [FeFe]‐Hydrogenase Mimics: Towards Photocatalytic Dyads for Hydrogen Production

AbstractSynthetic strategies towards molecular dyads based on peri‐substituted dichalcogenide (S,Se) [FeFe]‐hydrogenase synthetic mimics covalently linked to a ZnTPP photosensitizer are described. Dithiolate and diselenolate model systems 2–5 are prepared through condensation of 2‐naphthaldehydes with p‐methoxyaniline, reduction of the resulting Schiff base and oxidative insertion of Fe2(CO)6 into the dichalcogen bond of the imine or amine. Diselenolate‐based [FeFe] complexes (imine 3 and amine 5) are more efficient in electrocatalysis of proton reduction than their sulfur analogues 2 and 4 with increasing concentrations of pTsOH. Molecular dyad 1 containing a peri‐substituted naphthalene dithiolate Fe2(CO)6 cluster covalently linked via an amine to ZnTPP is prepared through sequential zinc insertion into the porphyrin followed by iron insertion into the disulfide bond.

Crystal structure of seleno-l-cystine di-hydro-chloride.

Numerous crystal structures are available for the dimeric amino acid cystine. In proteins it is formed by oxidation of the -SH thiol groups of two closely spaced cysteine residues, resulting in the formation of a familiar di-sulfide bridge. The title compound [systematic name: (R,R)-1,1'-dicarb-oxy-2,2'-(diselanedi-yl)diethanaminium dichloride], C6H14N2O4Se2 (2+)·2Cl(-), is the first example of a small mol-ecule structure of the biologically important analogue with a -CH2-Se-Se-CH2- bridging unit. Bond lengths and angles of seleno-l-cystine di-hydro-chloride and its isotypic sulfur analogue l-cystine di-hydro-chloride are compared.

Organochalcogen stabilizers efficiently protect model polyolefins exposed to chlorinated media

The small amounts of chlorine dioxide that are routinely supplemented to drinking water as a disinfectant also cause a degradation of the polyolefin pipes that are used for distribution of the water. Commonly used phenolic antioxidants can extend the service life of the polymer but the expected lifetime is still much shorter than desired (50 years) due to depletion of the antioxidant in the surface zone exposed to the aqueous solution. In search for better stabilizers for the pipes, we have tested an organotellurium compound, 4-(N,N-dimethylamino)phenyl 3-phenoxypropyl telluride (1), as well as its corresponding selenium and sulphur analogues and a series of organotellurium compounds where the electron density at the heteroatom was varied. Stabilizers were dissolved in squalane, which is a liquid hydrocarbon that could serve as a model for a polyolefin. The oxidation induction time (OIT), determined after exposure of the squalane solution to an aqueous solution of 10 ppm of chlorine dioxide for various times was determined by DSC to indicate the loss of antioxidant protection. Whereas Irganox 1010 was only effective as a stabilizer for a few hours, many of the organochalcogen compounds were considerably more resistant (>91 h for compound 1) towards chlorine dioxide.Thermogravimetric analyses of antioxidants indicated insignificant decomposition below 200 °C and increasing stability for the lighter chalcogen compounds (telluride < selenide < sulfide). Among organotelluriums, stability increases with increasing electron density at the heteroatom. Oxidation potentials of stabilizers as determined by cyclic voltammetry correlated fairly well with their protective effect in squalane (OIT-values). We therefore hypothesize that these compounds act primarily as electron donors towards peroxyl radicals. As determined by 125Te NMR-spectroscopy, organotellurium compound 1 in the presence of an excess of chlorine dioxide failed to produce an oxidation product. This may be the clue to its long-lasting protective effect in the squalane-assay.

Reactivity of selenium-containing compounds with myeloperoxidase-derived chlorinating oxidants: Second-order rate constants and implications for biological damage

Hypochlorous acid (HOCl) and N-chloramines are produced by myeloperoxidase (MPO) as part of the immune response to destroy invading pathogens. However, MPO also plays a detrimental role in inflammatory pathologies, including atherosclerosis, as inappropriate production of oxidants, including HOCl and N-chloramines, causes damage to host tissue. Low molecular mass thiol compounds, including glutathione (GSH) and methionine (Met), have demonstrated efficacy in scavenging MPO-derived oxidants, which prevents oxidative damage in vitro and ex vivo. Selenium species typically have greater reactivity toward oxidants compared to the analogous sulfur compounds, and are known to be efficient scavengers of HOCl and other hypohalous acids produced by MPO. In this study, we examined the efficacy of a number of sulfur and selenium compounds to scavenge a range of biologically relevant N-chloramines and oxidants produced by both isolated MPO and activated neutrophils and characterized the resulting selenium-derived oxidation products in each case. A dose-dependent decrease in the concentration of each N-chloramine was observed on addition of the sulfur compounds (cysteine, methionine) and selenium compounds (selenomethionine, methylselenocysteine, 1,4-anhydro-4-seleno-L-talitol, 1,5-anhydro-5-selenogulitol) studied. In general, selenomethionine was the most reactive with N-chloramines (k2 0.8–3.4×103M–1 s–1) with 1,5-anhydro-5-selenogulitol and 1,4-anhydro-4-seleno-L-talitol (k2 1.1–6.8×102M–1 s–1) showing lower reactivity. This resulted in the formation of the respective selenoxides as the primary oxidation products. The selenium compounds demonstrated greater ability to remove protein N-chloramines compared to the analogous sulfur compounds. These reactions may have implications for preventing cellular damage in vivo, particularly under chronic inflammatory conditions.

Efficient access to novel 5-aryloyl-1H-pyrano[2,3-d:6,5-d']dipyrimidine-2,4,6,8(3H,5H,7H,9H)-tetraones and their sulfur analogs in water

An efficient chemoselective synthesis of novel subs tituted pyrano(2,3-d)pyrimidines is described. A number of pyrano(2,3-d:6,5-d' )dipyrimidine-2,4,6,8(3 H,5 H,7 H,9 H)-tetraones and their sulfur analogs were synthesized through a one -pot condensation of arylglyoxal monohydrates with barbituric acid and thiobarbituri c acid in the presence of excess ammonium acetate in water at room temperature, affording the desired products in moderate to good yields.

Theoretical spectroscopic characterization at low temperatures of methyl hydroperoxide and three S-analogs.

The low temperature spectra of the detectable species methyl hydroperoxide (CH3OOH) and three sulfur analogs, the two isomers of methanesulfenic acid (CH3SOH and CH3OSH) and the methyl hydrogen disulfide (CH3SSH), are predicted from highly correlated ab initio methods (CCSD(T) and CCSD(T)-F12). Rotational parameters, anharmonic frequencies, torsional energy barriers, torsional energy levels, and their splittings are provided. Our computed parameters should help for the characterization and the identification of these organic compounds in laboratory and in the interstellar medium.

Distribution of selenoglucosinolates and their metabolites in Brassica treated with sodium selenate.

In Brassica species, hydrolysis of (methylthio)glucosinolates produces sulfur-containing aglycons which have demonstrated anticancer benefits. Selenized Brassicaceae contain (methylseleno)glucosinolates and their selenium-containing aglycons. As a prelude to biological testing, broccoli, cauliflower, and forage rape plants were treated with sodium selenate and their tap roots, stems, leaves, and florets analyzed for selenoglucosinolates and their Se aglycons. Two new selenoglucosinolates were identified: glucoselenoraphanin in broccoli florets and glucoselenonasturtiin in forage rape roots. A new aglycon, selenoberteroin nitrile, was identified in forage rape. The major selenoglucosinolates were glucoselenoerucin in broccoli, glucoselenoiberverin in cauliflower, and glucoselenoerucin and glucoselenoberteroin in forage rape roots. In broccoli florets, the concentrations of selenglucosinolates exceeded those of their sulfur analogues. Fertilization with selenium slightly reduced (methylthio)glucosinolates and aglycons in the roots, but increased them in the florets, the leaves, and sometimes the stems. These discoveries provide a new avenue for investigating how consumption of Brassica vegetables and their organoselenides may promote human health.

A mechanistic investigation of anti-elimination in (Z)-1,2-bis(arylseleno)-1-alkenes and their sulfur analogs.

The oxidation of (Z)-1,2-bis(arylseleno)-1-alkenes is known to afford alkynyl selenoxides via a unique selenoxide anti-elimination mechanism; however, to date, there have been no mechanistic studies of this reaction. During our studies of this transformation, monoselenoxides 6 and 7 were unexpectedly isolated as stable reaction intermediates. In addition, (77)Se NMR studies of the reaction mixture revealed the presence of an intramolecular Se···O interaction and the formation of alkynyl selenoxides. Meanwhile, even at higher temperatures, the reaction of a (Z)-1,2-bis(arylsulfinyl)-1-alkene, the sulfur analog of (Z)-1,2-bis(arylseleninyl)-1-alkenes, did not proceed via sulfoxide elimination but proceeded via isomerization and disproportionation. Therefore, the intramolecular Se···O interaction can be concluded to play a pivotal role in the anti-elimination reaction.

Effect of dynamic disorder on charge carrier dynamics in Ph4DP and Ph4DTP molecules

Electronic structure calculations were used to study the charge transport and optical properties of 2,2′,6,6′-tetraphenyldipyranylidene (Ph4DP) and its sulfur analogue 2,2′,6,6′-tetraphenyldithiopyranylidene (Ph4DTP) based molecules.

Improved selectivity for Pb(II) by sulfur, selenium and tellurium analogues of 1,8-anthraquinone-18-crown-5: synthesis, spectroscopy, X-ray crystallography and computational studies.

We report here a series of heteroatom-substituted macrocycles containing an anthraquinone moiety as a fluorescent signaling unit and a cyclic polyheteroether chain as the receptor. Sulfur, selenium, and tellurium derivatives of 1,8-anthraquinone-18-crown-5 (1) were synthesized by reacting sodium sulfide (Na2S), sodium selenide (Na2Se) and sodium telluride (Na2Te) with 1,8-bis(2-bromoethylethyleneoxy)anthracene-9,10-dione in a 1 : 1 ratio. The optical properties of the new compounds are examined and the sulfur and selenium analogues produce an intense green emission enhancement upon association with Pb(II) in acetonitrile. Selectivity for Pb(II) is markedly improved as compared to the oxygen analogue 1 which was also competitive for Ca(II) ion. UV-Visible and luminescence titrations reveal that 2 and 3 form 1 : 1 complexes with Pb(II), confirmed by single-crystal X-ray studies where Pb(II) is complexed within the macrocycle through coordinate covalent bonds to neighboring carbonyl, ether and heteroether donor atoms. Cyclic voltammetry of 2-8 showed classical, irreversible oxidation potentials for sulfur, selenium and tellurium heteroethers in addition to two one-electron reductions for the anthraquinone carbonyl groups. DFT calculations were also conducted on 1, 2, 3, 6, 6 + Pb(II) and 6 + Mg(II) to determine the trend in energies of the HOMO and the LUMO levels along the series.

Cyclization of thiocarbonyl groups in binuclear homoleptic nickel thiocarbonyls to give ligands derived from sulfur analogues of croconic and rhodizonic acids.

The sulfur analogue of the well-known Ni(CO)4, namely, Ni(CS)4, has been observed spectroscopically in low temperature matrices but is not known as a stable species under ambient conditions. Theoretical studies show that Ni(CS)4 with monomeric CS ligands and tetrahedrally coordinated nickel is disfavored by ∼17 kcal/mol relative to unusual isomeric Ni(C2S2)2 structures. In the latter structures the CS ligands couple pairwise through C-C bond formation to give dimeric S═C═C═S ligands, which bond preferentially to the nickel atom through their C═S bonds rather than their C═C bonds. Coupling of CS ligands in the lowest energy binuclear Ni2(CS)n (n = 7, 6, 5) structures results in cyclization to give remarkable CnSn (n = 5, 6) ligands containing five- and six-membered carbocyclic rings. Such ligands, which are the sulfur analogues of the well-known croconate (n = 5) and rhodizonate (n = 6) oxocarbon ligands, function as bidentate ligands to the central Ni2 unit. Higher energy Ni2(CS)n (n = 7, 6, 5) structures contain dimeric C2S2 ligands, which can bridge the central Ni2 unit. Dimeric C2S2 ligands rather than tetrathiosquare C4S4 ligands are found in the lowest energy Ni2(CS)4 structures.

Poly(thieno[3,4-b]-1,4-oxathiane): medium effect on electropolymerization and electrochromic performance.

The asymmetrical sulfur analog of 3,4-ethylenedioxythiophene (EDOT), thieno[3,4-b]-1,4-oxathiane (EOTT), was synthesized, and its electropolymerization was comparatively investigated by employing different solvent-electrolyte systems (room temperature ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate (BmimPF6), CH2Cl2-Bu4NPF6, and CH2Cl2-BmimPF6). Further, the effect of solvents and supporting electrolytes on the structure, morphology, electrochemical, electronic, and optical properties and electrochromic performance of the obtained poly(thieno[3,4-b]-1,4-oxathiane) (PEOTT) films were minutely studied. PEOTT film with a band gap (Eg) of about 1.6 eV could be facilely electrodeposited in all the solvent-electrolytes and displayed excellent electroactivity, outstanding redox stability in a wide potential window, and improved thermal stability. Cyclic voltammetry showed that EOTT could be electropolymerized at a lower oxidation potential in BmimPF6 (∼1.0 V vs Ag/AgCl) due to several advantanges of RTIL BmimPF6 itself, such as high intrinsic conductivity and mild chemical conditions, etc., and the resulting PEOTT film exhibited compact morphology with better electroactivity and stability and higher electrical conductivity. On the other hand, PEOTT films from all the sovent-electrolytes also showed the electrochromic nature by color changing from gray blue to green, and further kinetic studies revealed that PEOTT had decent contrast ratios (36%), higher coloration efficiencies (212 cm(2)/C in BmimPF6), low switching voltages, moderate response time (1.2 s), excellent stability, and color persistence. From these results, PEOTT provides more plentiful electrochromic colors and holds promise for display applications.