Stable Nitroxide Research Articles

First α-deuterium nitroxides; synthesis and EPR study

Herein is reported the first preparation of stable α-deuterium nitroxides of the IAPNO family. The confirmation and characteristics of the α-deuterium nitroxides and their α-hydrogen analogues are compared and analyzed. Such α-deuterium nitroxides may find use in biology, medicine and physical chemistry.

Synthesis and Characterization of Two Chiral Pyrrolyl α-Nitronyl Nitroxide Radicals and Determination of their Cytotoxicity and Radioprotective Properties in C6 Cells and Mice under Ionizing Radiation

In this study, two chiral nitronyl nitroxyl radicals, L1 and D1, were synthesized and evaluated for their potential radioprotective properties invitro and invivo. We synthesized the new stable nitronyl nitroxide radicals, L1 and D1, according to Ullman’s method, and their chemical structures were characterized using UV-vis absorption, electron spin resonance (ESR), and circular dichroism (CD) spectra. The cytotoxicity of L1 and D1 on C6 glioma cells (C6 cells) was examined using the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay. To study the anti-radiation effects of L1 and D1 on C6 cells, we determined the optical density (OD) values of irradiated C6 cells using the MTT assay. The effects of L1 and D1 on the survival rate of mice after radiation exposure was evaluated. To demonstrate the influence of L1 and D1 pre-treatment on the antioxidant enzyme system, we studied the activities of superoxide dismutase (SOD), catalase (CAT), malondialdehyde (MDA), and glutathione peroxidase (GSH) in mouse plasma after exposure to 6.5 Gy gamma radiation. The results showed that L1 and D1 did not have any obvious cytotoxicity at concentrations below 125μgmL−1. Moreover, L1 and D1 had the same cytotoxic effects on C6 cells. L1 and D1 significantly enhanced C6 cell survival after 8, 10, and 12 Gy radiation exposure, and there was no significant difference in the OD values between L1 and D1. The effects of these drugs on mouse survival rates were dose-dependent. Pre-treatment with different concentrations of L1, D1, or WR2721 significantly increased the activity of SOD, CAT, and GSH and significantly decreased the activity of MDA compared with radiation exposure only. In addition, the activities of SOD, CAT, and GSH in the L1 group were higher than those in the D1 group, whereas the activity of MDA was lower. Therefore, L1 and D1 have potential as safe and efficient therapeutic drugs against radiation damage.

Synthesis and characterisation of redox hydrogels based on stable nitroxide radicals.

The principle of encapsulation/release of a guest molecule from stimuli responsive hydrogels (SRHs) is mainly realised with pH, temperature or light stimuli. However, only a limited number of redox responsive hydrogels have been investigated so far. We report here the development of a SRH that can release its guest molecule upon a redox stimulus. To obtain this redox hydrogel, we have introduced into the hydrogel the 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) stable nitroxide radical, which can be reversibly oxidized into an oxoammonium cation (TEMPO+). Water solubility is provided by the presence of the (oligoethyleneglycol)methacrylate (OEGMA) comonomer. Electrochemical and mechanical characterization showed that those gels exhibit interesting physicochemical properties, making them very promising candidates for practical use in a wide range of applications.

Plasma Polymerization of TEMPO Yields Coatings Containing Stable Nitroxide Radicals for Controlling Interactions with Prokaryotic and Eukaryotic Cells

Stable organic nitroxide radicals have been shown to exhibit similar cell biology signaling properties as the well-known but short-lived small molecule nitric oxide, such as affecting intracellular...

Interaction Kinetics of Sulfadiazine and N-Acetyl-sulfadiazine with Soil Humic Acid: ESR Investigations with Nitroxide Spin Label

The interaction of sulfadiazine (SDZ) and its main metabolite N-acetyl-SDZ (N-ac-SDZ) with model humic acid was investigated with stable paramagnetic nitroxide spin probes. Leonardite humic acid (LHA) was mixed with laccase to enhance the amount of reactive quinone groups of LHA and then incubated with nitroxide spin-labelled analogs of SDZ and N-ac-SDZ. The labeling at the pyrimidine moiety of SDZ leaves the aniline moiety susceptible to covalent binding to LHA, which is blocked by the N-acetylation. A broadened electron spin resonance (ESR) signal was observed for SDZ, which increased immediately after incubation and indicates strong restriction of the re-orientational motion of the spin probe, i.e., immobilization due covalent binding of the aniline moiety of SDZ to reactive quinone sites of LHA. A fast first-order reaction with a time constant of 17.6 ± 3.4 h of covalent binding was determined. The broadened ESR signal of N-ac-SDZ declined immediately after incubation with LHA and is caused by unspecific sorption to LHA, not by covalent binding. Short time constants of the bound and free SDZ were found for the reduction by the antioxidant sodium ascorbate demonstrating that SDZ and N-ac-SDZ are not physically entrapped by LHA.

Triplet-state spin labels for highly sensitive pulsed dipolar spectroscopy

ABSTRACTPulsed dipolar spectroscopic methods allow nanometer distance measurements between pairs of spin labels. We have proposed a new spin labelling approach, based on the population of a chromophore triplet under light excitation, testing it on a peptide-based spectroscopic ruler and a photosynthetic protein. We have applied a modified Pulsed Electron DOuble Resonance (PELDOR) sequence where the photogeneration of the triplet spin precedes the conventional 4-pulse PELDOR sequence. In this experiment, the triplet-state serves as detection spin while the stable nitroxide is the pump spin. Alternatively, a new method, Laser-Induced Magnetic Dipole spectroscopy (LaserIMD), has been proposed: the nitroxide signal is detected while a time varying laser pulse acts as a pump to generate the triplet state [C. Hintze, D. Bücker, S. Domingo Köhler, G. Jeschke and M. Drescher, J. Phys. Chem. Lett. 7 (12), 2204 (2016)]. For the first time, in this work, we compare the two dipolar techniques performing X-band experiments in the same experimental conditions and deriving analytical expressions for the echo modulation by the density matrix formalism.

Synthesis and characterization of electroactive PEDOT-TEMPO polymers as potential cathode materials in rechargeable batteries

Herein we report a novel series of conjugated polymers bearing stable nitroxide pendant groups for possible applications as cathode-active material in secondary batteries. The polymers comprise a 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) moiety immobilized on a poly(3,4-ethylenedioxythiophene) (PEDOT) backbone via ester groups (PEDOT-TEMPO P1 and PEDOT-diTEMPO P2). The multistep synthesis of the corresponding monomers and their chemical characterization are described. Furthermore, oxidative electrochemical and chemical polymerization were performed in order to synthesize polymers on gram-scale for battery tests and to investigate their electrochemical behaviour, respectively. In addition, the electrochemical properties of polymer P1 were studied by potentiodynamic and galvanostatic methods. The results demonstrate that the as-synthesized nitroxide radical polymers showed an electrochemically reversible redox reaction of the TEMPO radicals at 3.5 V vs Li/Li+. When used as cathode material in galvanostatic cycling tests, P1 exhibited a moderate initial specific capacity of 47 mA h g−1 (62% of the theoretical capacity) which slowly fades to 38 mA h g−1 within 50 cycles.

Pro-fluorescent mitochondria-targeted real-time responsive redox probes synthesised from carboxy isoindoline nitroxides: Sensitive probes of mitochondrial redox status in cells

Here we describe new fluorescent probes based on fluorescein and rhodamine that provide reversible, real-time insight into cellular redox status. The new probes incorporate bio-imaging relevant fluorophores derived from fluorescein and rhodamine linked with stable nitroxide radicals such that they cannot be cleaved, either spontaneously or enzymatically by cellular processes. Overall fluorescence emission is determined by reversible reduction and oxidation, hence the steady state emission intensity reflects the balance between redox potentials of critical redox couples within the cell. The permanent positive charge on the rhodamine-based probes leads to their rapid localisation within mitochondria in cells. Reduction and oxidation also leads to marked changes in the fluorophore lifetime, enabling monitoring by fluorescence lifetime imaging microscopy. Finally, we demonstrate that administration of a methyl ester version of the rhodamine-based probe can be used at concentrations as low as 5 nM to generate a readily detected response to redox stress within cells as analysed by flow cytometry.

Magnetic Exchange Interaction in Nitronyl Nitroxide Radical-Based Single Crystals of 3d Metal Complexes: A Combined Experimental and Theoretical Study.

Two stable nitronyl nitroxide free radicals {R1 = 4′-methoxy-phenyl-4,4,5,5,-tetramethylimidazoline-1-oxyl-3-oxide (NNPhOMe) and R2 = 2-(2′-thienyl)-4,4,5,5-tetramethylimidazoline 3-oxide 1-oxyl (NNT)} are successfully synthesized using Ullmann condensation. The reactions of these two radicals with 3d transition metal ions, in the form of M(hfac)2 (where M = Co or Mn, hfac: hexafluoroacetylacetone), result in four metal–organic complexes Co(hfac)2(NNPhOMe)2, 1; Co(hfac)2(NNT)2·(H2O), 2; Mn(hfac)2(NNPhOMe)·x(C7H16), 3; and Mn(hfac)2(NNT)2, 4. The crystal structure and magnetic properties of these complexes are investigated by single-crystal X-ray diffraction, dc magnetization, infrared, and electron paramagnetic resonance spectroscopies. The compounds 1 and 4 crystallize in the triclinic, P1̅, space group, whereas complex 3 crystallizes in the monoclinic structure with the C2/c space group and forms chain-like structure along the c direction. The complex 2 crystallizes in the monoclinic symmetry with the P21/c space group in which the N–O unit of the radical coordinates with the Co ion through hydrogen bonding of a water molecule. All compounds exhibit antiferromagnetic interactions between the transition metal ions and nitronyl nitroxide radicals. The magnetic exchange interactions (J/KB) are derived using isotropic spin Hamiltonian H = −2J∑(SmetalSradical) for the model fitting to the magnetic susceptibility data for 1, 2, 3, and 4. The exchange interaction strengths are found to be −328, −1.25, −248, and −256 K, for the 1, 2, 3, and 4 metal–organic complexes, respectively. Quantum chemical density functional theory (DFT) computations are carried out on several models of the metal–radical complexes to elucidate the magnetic interactions at the molecular level. The calculations show that a small part of the inorganic spins are delocalized over the oxygens from hfac {∼0.03 for Co(II) and ∼0.015 for Mn(II)}, whereas a more significant fraction {∼0.24 for Mn(II) and ∼0.13 for Co(II)} of delocalized spins from the metal ion is transferred to the coordinated oxygen atom(s) of nitronyl nitroxide.

Translational repression of HIF2α expression in mice with Chuvash polycythemia reverses polycythemia.

Chuvash polycythemia is an inherited disease caused by a homozygous germline VHLR200W mutation, which leads to impaired degradation of HIF2α, elevated levels of serum erythropoietin, and erythrocytosis/polycythemia. This phenotype is recapitulated by a mouse model bearing a homozygous VhlR200W mutation. We previously showed that iron-regulatory protein 1-knockout (Irp1-knockout) mice developed erythrocytosis/polycythemia through translational derepression of Hif2α, suggesting that IRP1 could be a therapeutic target to treat Chuvash polycythemia. Here, we fed VhlR200W mice supplemented with Tempol, a small, stable nitroxide molecule and observed that Tempol decreased erythropoietin production, corrected splenomegaly, normalized hematocrit levels, and increased the lifespans of these mice. We attribute the reversal of erythrocytosis/polycythemia to translational repression of Hif2α expression by Tempol-mediated increases in the IRE-binding activity of Irp1, as reversal of polycythemia was abrogated in VhlR200W mice in which Irp1 was genetically ablated. Thus, a new approach to the treatment of patients with Chuvash polycythemia may include dietary supplementation of Tempol, which decreased Hif2α expression and markedly reduced life-threatening erythrocytosis/polycythemia in the VhlR200W mice.

Design, synthesis and biological evaluation of hybrid nitroxide-based non-steroidal anti-inflammatory drugs

Dual-acting hybrid anti-oxidant/anti-inflammatory agents were developed employing the principle of pharmacophore hybridization. Hybrid agents were synthesized by combining stable anti-oxidant nitroxides with conventional non-steroidal anti-inflammatory drugs (NSAIDs). Several of the hybrid nitroxide-NSAID conjugates displayed promising anti-oxidant and anti-inflammatory effects on two Non-Small Cell Lung Cancer (NSCLC) cells (A549 and NCI-H1299) and in ameliorating oxidative stress induced in 661 W retinal cells. One ester-linked nitroxide-aspirin analogue (27) delivered better anti-inflammatory effects (cyclooxygenase inhibition) than the parent compound (aspirin), and also showed similar reactive oxygen scavenging activity to the anti-oxidant, Tempol. In addition, a nitroxide linked to the anti-inflammatory drug indomethacin (39) significantly ameliorated the effects of oxidative stress on 661 W retinal neurons at efficacies greater or equal to the anti-oxidant Lutein. Other examples of the hybrid conjugates displayed promising anti-cancer activity, as demonstrated by their inhibitory effects on the proliferation of A549 NSCLC cells.

Comparative Genotoxicity of TEMPO and 3 of Its Derivatives in Mouse Lymphoma Cells.

TEMPO (2, 2, 6, 6-tetramethylphiperidine-1-oxyl) and its derivatives are stable free radical nitroxides widely used in the field of chemistry, biology, and pharmacology. TEMPO was previously found to be mutagenic and to induce micronuclei in mammalian cells. In this study, we investigated and quantified the genotoxicity of 4 structurally similar nitroxides, TEMPO and 3 of its derivatives (4-hydroxy-TEMPO, 4-oxo-TEMPO, and 4-methoxy-TEMPO), using the mouse lymphoma assay (MLA) and Comet assay in L5178Y Tk+/- cells. The results showed that all tested nitroxides were cytotoxic and mutagenic in the MLA, both in the presence and absence of S9, with metabolic activation significantly enhancing the cytotoxicity and/or mutagenicity. In addition, the 4 nitroxides caused DNA-strand breakage. The mutagenicity and DNA damaging dose-responses of the test articles were compared using the PROAST benchmark dose software package. The potency ranking of the 4 nitroxides for mutagenicity was different from the ranking of the DNA damaging effects. The mode of action analysis by a multi-endpoint DNA damage pathway assay classified all 4 nitroxides as clastogens. In addition, the majority of the induced Tk mutants showed loss of heterozygosity at the Tk and D11Mit42 loci (ie, chromosome damage <31 Mbp). These results suggest that TEMPO and its 3 derivatives are cytotoxic and mutagenic in mouse lymphoma cells through a mechanism that involves strand breakage and large alterations to DNA. The potency rankings indicate that the different TEMPO derivatives vary in their mutagenic and DNA damaging potential.

Electron Paramagnetic Resonance Measurements of Reactive Oxygen Species by Cyclic Hydroxylamine Spin Probes.

Oxidative stress contributes to numerous pathophysiological conditions such as development of cancer, neurodegenerative, and cardiovascular diseases. A variety of measurements of oxidative stress markers in biological systems have been developed; however, many of these methods are not specific, can produce artifacts, and do not directly detect the free radicals and reactive oxygen species (ROS) that cause oxidative stress. Electron paramagnetic resonance (EPR) is a unique tool that allows direct measurements of free radical species. Cyclic hydroxylamines are useful and convenient molecular probes that readily react with ROS to produce stable nitroxide radicals, which can be quantitatively measured by EPR. In this work, we critically review recent applications of various cyclic hydroxylamine spin probes in biology to study oxidative stress, their advantages, and the shortcomings. Recent Advances: In the past decade, a number of new cyclic hydroxylamine spin probes have been developed and their successful application for ROS measurement using EPR has been published. These new state-of-the-art methods provide improved selectivity and sensitivity for in vitro and in vivo studies. Although cyclic hydroxylamine spin probes EPR application has been previously described, there has been lack of translation of these new methods into biomedical research, limiting their widespread use. This work summarizes "best practice" in applications of cyclic hydroxylamine spin probes to assist with EPR studies of oxidative stress. Additional studies to advance hydroxylamine spin probes from the "basic science" to biomedical applications are needed and could lead to better understanding of pathological conditions associated with oxidative stress. Antioxid. Redox Signal. 28, 1433-1443.

Simultaneous Introduction of Two Nitroxides in the Reaction: A New Approach to the Synthesis of Heterospin Complexes.

A new approach to the synthesis of multispin compounds has been developed, namely, the simultaneous introduction of two different stable nitroxides (nitronyl nitroxide and imino nitroxide) in a reaction with a metal ion. An important characteristic of the new method is that nitronyl nitroxide and imino nitroxide introduced in the reaction with the metal are the products of different series; i.e., the nitronyl nitroxide molecule differs from the imino nitroxide molecule not only in one additional oxygen molecule per molecule but also in another substituent in the side chain of the organic paramagnet. This possibility was demonstrated on the synthesis of multispin compounds [Ni2(A1)(L2)2(Piv)(MeOH)], [Ni2(L1)(A2)2(Piv)(H2O)], [Co2(A1)(L2)2(Piv)(MeOH)], and [Co3(L1)2(A2)2(Piv)2], in which Ln and An differ in the substituent in the phenyl ring. The number of multispin compounds that can be synthesized by the proposed method is almost unlimited. The heterospin complexes of transition metals with coordinated nitronyl nitroxide and imino nitroxide in one molecule contain energy-different exchange interaction channels that differ in both magnitude and sign, as confirmed by the quantum-chemical analysis of exchange channels in [Ni(B1)(B2)2](NO3)2. The series of mixed-radical complexes may include compounds with nontrivial magnetic properties such as [Co2(A1)(L2)2(Piv)(MeOH)], which experiences bulk magnetic ordering below 3.5 K.

ROS generation and JNK activation contribute to 4-methoxy-TEMPO-induced cytotoxicity, autophagy, and DNA damage in HepG2 cells.

4-Methoxy-TEMPO, a derivative of 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO), is a stable nitroxide radical and is generally used in organic and pharmaceutical syntheses for the oxidation of alcohols. Previously, we reported the involvement of reactive oxygen species (ROS) and c-Jun N-terminal kinases (JNK) in TEMPO-induced apoptosis in mouse L5178Y cells. In this study, we investigated 4-methoxy-TEMPO induced toxicity in human HepG2 hepatoma cells and its underlying mechanisms. Treatments with 4-methoxy-TEMPO (0.5-5mM for 2-6h) caused oxidative stress as demonstrated by increased intensity of the ROS indicator H2DCF-DA, decreased levels of glutathione. 4-Methoxy-TEMPO treatment also induced DNA damage as characterized by increased levels of DNA tail intensity in the Comet assay, increased phosphorylation of related proteins including γ-H2A.X, p-Chk1, and p-Chk2, and activation of MAPK signaling pathways. In addition, 4-methoxy-TEMPO also induced autophagy as demonstrated by the conversion of LC3B-I to II, decreased level of p62, and the appearance of GFP-LC3B punctae. To investigate the crosstalk between different signaling pathways, pretreatment of HepG2 with N-acetylcysteine, an ROS scavenger, attenuated 4-methoxy-TEMPO-induced DNA damage, suppressed JNK activation, and diminished autophagy induction. Furthermore, inhibiting JNK activation by a JNK-specific inhibitor, SP600125, decreased DNA damage levels induced by 4-methoxy-TEMPO. These results suggest that multiple mechanisms including ROS generation, DNA damage, and MAPK activation contribute to 4-methoxy-TEMPO-induced toxicity.

Probing Gas Adsorption in Metal–Organic Framework ZIF-8 by EPR of Embedded Nitroxides

Metal–organic frameworks (MOFs) are being increasingly considered as promising materials for gas separation and storage, yet specific interactions between gas molecules and the inner surface of pores are still not well understood. In this work, we propose a new approach for investigation of such interactions by Electron Paramagnetic Resonance (EPR). We use stable nitroxide radicals as multifunctional agents embedded into the pores of a MOF prior to the gas sorption. They act as EPR-active reporters, and simultaneously as competitor molecules during the gas adsorption process. We exemplify this approach using a ZIF-8 framework, nitroxide TEMPO ((2,2,6,6-tetramethylpiperidin-1-yl)oxyl), and CO2, N2, and O2 gases. The mobility of nitroxide monitored by continuous wave EPR behaves differently upon adsorption of each of these gases. In particular, a noticeable increase of mobility in the presence of CO2 reveals the weakening of guest–host interactions TEMPO–MOF induced by CO2, which was qualitatively supported by molecular dynamic calculations. The nitroxides can be embedded in MOFs postsynthetically, and their negligible amounts (≤1 per 1000 cells) are required due to a high sensitivity of EPR. Therefore, the proposed approach is sufficiently versatile and might find broad applications for various MOFs.

Design, Synthesis, and Characterization of Polyphosphazene Bearing Stable Nitroxide Radicals as Cathode-Active Materials in Li-Ion Batteries

A new synthetic strategy is developed for the synthesis of polyphosphazene bearing stable nitroxide radicals as a pendant group. The resulting material is investigated as a cathode-active material for rechargeable lithium–ion batteries that performs 80 mAh g−1 capacities at a C/2 current density over 50 cycles. Thus, the inorganic–organic hybrid system can be proposed as an alternative cathode-active material with improved performance.

Mechanism of HRP-catalyzed nitrite oxidation by H2O2 revisited: Effect of nitroxides on enzyme inactivation and its catalytic activity

The peroxidative activity of horseradish peroxidase (HRP) undergoes progressive inactivation while catalyzing the oxidation of nitrite by H2O2. The extent of inactivation increases as the pH increases, [nitrite] decreases or [H2O2] increases, and is accompanied by a loss of the Soret peak of HRP along with yellow-greenish coloration of the solution. HRP-catalyzed nitrite oxidation by H2O2 involves not only the formation of compounds I and II as transient heme species, but also compound III, all of which in turn, oxidize nitrite yielding •NO2. The rate constant of nitrite oxidation by compound III is at least 10-fold higher than that by compound II, which is also reducible by •NO2 where its reduction by nitrite is the rate-determining step of the catalytic cycle. The extent of the loss of the Soret peak of HRP is lower than the loss of its peroxidative activity implying that deterioration of the heme moiety leading to iron release only partially contributes toward heme inactivation. Cyclic stable nitroxide radicals, such as 2,2,6,6-tetramethyl-piperidine-N-oxyl (TPO), 4-OH-TPO and 4-NH2-TPO at µM concentrations detoxify •NO2 thus protecting HRP against inactivation mediated by this radical. Hence, HRP inactivation proceeds via nitration of the porphyrin ring most probably through compound I reaction with •NO2, which partially leads to deterioration of the heme moiety. The nitroxide acts catalytically since its oxidation by •NO2 yields the respective oxoammonium cation, which is readily reduced back to the nitroxide by H2O2, superoxide ion radical, and nitrite. In addition, the nitroxide catalytically inhibits tyrosine nitration mediated by HRP/H2O2/nitrite reactions system as it efficiently competes with tyrosyl radical for •NO2. The inhibition by nitroxides of tyrosine nitration is demonstrated also in the case of microperoxidase (MP-11) and cytochrome c revealing an additional role played by nitroxide antioxidants.

Superoxide radicals in the kinetics of nitroxide-inhibited oxidation of methyl linoleate in micelles

The kinetics of the oxidation of methyl linoleate in micelles inhibited by stable nitroxides under the conditions of initiation by superoxide radicals was studied. Multiple breakdown of the oxidation chains was observed in this process. The antioxidant activity of nitroxides increased when the reduction potential of the oxoammonium cation/nitroxide pair decreased and their lipophilicity increased.

Synthesis and Electrochemical Characterization of New Electro-Active Polymer Bearing TEMPO Functional Groups

Synthesis and electrochemical characterization of new electro-active polymer bearing TEMPO functional groups L.Assumaa, A.Santiagoa, Y. Kervallaa, JM. Mouescaa, V. Maurela, T. Gutelb, L. Duboisa, S. Sadkia a. INAC-SPrAM-SYMMES, bLITEN-DEHT-Laboratoire des Composants pour Batteries, CEA 17, rue des Martyrs, Grenoble Organic radical species, particularly pendant nitroxide radical polymers, have been explored as a cathode-active, charge-storage material for secondary Li-ion batteries1. However, nitroxide radical contained polymers are derivatives of conventional plastics, which are insulator, and a very large amount of conducting agents (such as carbon black, graphite, graphene and carbon fibers), even up to 60-80 wt% of the total electrode, is required in the fabrication of the composite electrode and this leads to a decrease of the composite electrode capacity2. In order to decrease de quantity of conducting agents we combined a stable nitroxide radical with a conductive polymer backbone constituted by 2,7-bisthiophene carbazole, which is characterized by high thermal stability and high conductivity. In this work we present the synthesis of this new electro-active conductive redox polymer, the electrochemical characterization, the ESR characterization and battery test. The previous results showed a very high electrochemical reversibility of this system, and a superposition between the redox potential of bisthiophene carbazole backbone and nitroxide radical . Moreover, the preliminary battery test displayed a good capacity (about 60 mAh / g) and a good life cycle, about 50 cycles for a discharge rate equals to C/10.. Thanks to these preliminary results, this polymer could be a viable alternative to the actual radical redox polymers. (1) Song, Z.; Hapshen Z., Energy and environmental Science 2013 , 60, 2280. (2) Lihuan X., Fang, Y., Chang, S., Lvlv Ji, Cheng Z., Electrochimica Acta, 2014, 130,148-155.