10 research outputs found

    Evaluating Ionic Liquids as Hypergolic Fuels: Exploring Reactivity from Molecular Structure

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    International audienceA total of 38 ionic liquids (19 of which are new) comprised of 13 cations, 1-propargyl-3-methyl-imidazolium, 1-allyl-3-methyl-imidazolium, 1,3-dimethyl-imidazolium, 1-ethyl-3-methyl-imidazolium, 1-butyl-3-methyl-imidazolium, 1-methoxyethyl-3-methyl-imidazolium, 1-methyl-4-butyl-1,2,4-triazolium, 1-methyl-4-allyl-1,2,4-triazolium, 1-methyl-4-amino-1,2,4-triazolium, N-butyl-N-methyl-pyrrolidinium, N-allyl-N-methyl-pyrrolidinium, N-allyl-pyridinium, and N-butyl-3-methyl-pyridinium, paired with three anions, dicyanamide, azide, and nitrocyanamide, have been prepared, characterized, and evaluated as potential hypergolic fuels by determining key physical, thermal, and ignition properties. The reactivity of these ionic liquids (32 liquids and 6 solids which melt below 100 degrees C) was strongly correlated to increased electron density in the cation, while small changes in physical properties had little effect beyond a certain threshold, suggesting that subtle changes in chemical reactivity can greatly influence the hypergolic ignition pathway

    Evaluating Ionic Liquids as Hypergolic Fuels: Exploring Reactivity from Molecular Structure

    No full text
    A total of 38 ionic liquids (19 of which are new) comprised of 13 cations, 1-propargyl-3-methyl-imidazolium, 1-allyl-3-methyl-imidazolium, 1,3-dimethyl-imidazolium, 1-ethyl-3-methyl-imidazolium, 1-butyl-3-methyl-imidazolium, 1-meth-oxyethyl-3-methyl-imidazolium, 1-methyl-4-butyl-1,2,4-triazolium, 1-methyl-4-allyl-1,2,4-triazolium, 1-methyl-4-amino-1,2,4-tri-azolium, <i>N</i>-butyl-<i>N</i>-methyl-pyrrolidinium, <i>N</i>-allyl-<i>N</i>-methyl-pyrrolidinium, <i>N</i>-allyl-pyridinium, and <i>N</i>-butyl-3-methyl-pyridinium, paired with three anions, dicyanamide, azide, and nitrocyanamide, have been prepared, characterized, and evaluated as potential hypergolic fuels by determining key physical, thermal, and ignition properties. The reactivity of these ionic liquids (32 liquids and 6 solids which melt below 100 °C) was strongly correlated to increased electron density in the cation, while small changes in physical properties had little effect beyond a certain threshold, suggesting that subtle changes in chemical reactivity can greatly influence the hypergolic ignition pathway

    Evaluating Ionic Liquids as Hypergolic Fuels: Exploring Reactivity from Molecular Structure

    No full text
    A total of 38 ionic liquids (19 of which are new) comprised of 13 cations, 1-propargyl-3-methyl-imidazolium, 1-allyl-3-methyl-imidazolium, 1,3-dimethyl-imidazolium, 1-ethyl-3-methyl-imidazolium, 1-butyl-3-methyl-imidazolium, 1-meth-oxyethyl-3-methyl-imidazolium, 1-methyl-4-butyl-1,2,4-triazolium, 1-methyl-4-allyl-1,2,4-triazolium, 1-methyl-4-amino-1,2,4-tri-azolium, <i>N</i>-butyl-<i>N</i>-methyl-pyrrolidinium, <i>N</i>-allyl-<i>N</i>-methyl-pyrrolidinium, <i>N</i>-allyl-pyridinium, and <i>N</i>-butyl-3-methyl-pyridinium, paired with three anions, dicyanamide, azide, and nitrocyanamide, have been prepared, characterized, and evaluated as potential hypergolic fuels by determining key physical, thermal, and ignition properties. The reactivity of these ionic liquids (32 liquids and 6 solids which melt below 100 °C) was strongly correlated to increased electron density in the cation, while small changes in physical properties had little effect beyond a certain threshold, suggesting that subtle changes in chemical reactivity can greatly influence the hypergolic ignition pathway

    Evaluating Ionic Liquids as Hypergolic Fuels: Exploring Reactivity from Molecular Structure

    No full text
    A total of 38 ionic liquids (19 of which are new) comprised of 13 cations, 1-propargyl-3-methyl-imidazolium, 1-allyl-3-methyl-imidazolium, 1,3-dimethyl-imidazolium, 1-ethyl-3-methyl-imidazolium, 1-butyl-3-methyl-imidazolium, 1-meth-oxyethyl-3-methyl-imidazolium, 1-methyl-4-butyl-1,2,4-triazolium, 1-methyl-4-allyl-1,2,4-triazolium, 1-methyl-4-amino-1,2,4-tri-azolium, <i>N</i>-butyl-<i>N</i>-methyl-pyrrolidinium, <i>N</i>-allyl-<i>N</i>-methyl-pyrrolidinium, <i>N</i>-allyl-pyridinium, and <i>N</i>-butyl-3-methyl-pyridinium, paired with three anions, dicyanamide, azide, and nitrocyanamide, have been prepared, characterized, and evaluated as potential hypergolic fuels by determining key physical, thermal, and ignition properties. The reactivity of these ionic liquids (32 liquids and 6 solids which melt below 100 °C) was strongly correlated to increased electron density in the cation, while small changes in physical properties had little effect beyond a certain threshold, suggesting that subtle changes in chemical reactivity can greatly influence the hypergolic ignition pathway

    Distribution of plasma fatty acids is associated with response to chemotherapy in non-Hodgkin's lymphoma patients

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    Our recent data have linked plasma phospholipid fatty acid (FA) profile in patients with non-Hodgkin's lymphoma (NHL) with the clinical stage and aggressiveness of the disease. Thus, we proposed that plasma FA status in these patients may influence the effect of chemotherapy. The aim of this work was to assess FA status in NHL patients undergoing chemotherapy in relation to their response to therapy. We analyzed plasma FA profile in 47 newly diagnosed NHL patients before chemotherapy, after 3 cycles and after the end of the planned chemotherapy. Patients were treated according to the hospital protocol: 28 patients with cyclophosphamide, doxorubicin, vincristine and prednisone, 7 with other anthracycline-containing regimens, 4 patients with cyclophosphamide, vincristine and prednisone and 8 with fludarabine-based regimens. Rituximab was added in 22 patients. Ten patients who did not receive all planned chemotherapy due to death or toxicity (non-completers) had significantly lower (p lt 0.05) baseline proportion of palmitoleic, linoleic, eicosapentaenoic and docosahexaenoic acid, as well as n-3 and n-6 FA, than the patients who completed chemotherapy (completers). Furthermore, the completers were divided according to the response to chemotherapy to complete remission (CR), stable disease and progressive disease (PD). Proportion of palmitic acid after the end of chemotherapy was the highest in the PD group, while stearic acid showed the opposite trend. Palmitoleic acid and all n-3 FA (18: 3, 20: 5, 22: 5 and 22: 6) were the highest in the patients in remission and the lowest in PD (p lt 0.001). Linoleic acid decreased and arachidonic acid increased from the CR to the PD group (p lt 0.001). These results suggest that aberrations in plasma FA may influence response to chemotherapy in patients with NHL

    Corporate Practices

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