Synthesis and phytotoxicity of new ionic liquids incorporating chiral cations and/or chiral anions

被引:47
作者
Balczewski, Piotr
Bachowska, Barbara
Bialas, Tomasz
Biczak, Robert
Wieczorek, Wanda M.
Balinska, Agnieszka
机构
[1] Polish Acad Sci, Ctr Mol & Macromol Studies, Dept Heteoorgan Chem, PL-90363 Lodz, Poland
[2] Jan Dlugosz Univ, Inst Chem & Environm Protect, PL-42200 Czestochowa, Poland
[3] Tech Univ Lodz, Inst Gen & Ecol Chem, PL-90924 Lodz, Poland
关键词
chiral ionic liquids; (-)-nopyl derivatives; phytotoxicity test; soil; environmental protection;
D O I
10.1021/jf062849q
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
The aim of this work was to synthesize chiral ionic liquids as chiral solvents for organic synthesis and to evaluate the phyto(eco)toxicity of the new products and starting N-alkylimidazoles and their potential environmental influence on soil and plants. Chiral ionic liquids containing anions such as Cl-, Br-, TsO-, PF6-, NO3-, CF3SO3-, and (+)- and (-)-C6H5CH(OH)C(O)O- were synthesized using (-)-(1R)-6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-ethyl [(-)-(1R)-nopyl] halides (X = Cl, Br) and tosylate in 62-100% yields. The chloride 7 and the nitrate 13 ionic liquids possessed a toxicity dependent on the applied concentration. The lowest concentration causing a distinct reduction in plant germination/growth was 100 mg/kg. Spring barley better tolerated the ionic liquids (200 mg/kg) than common radish (100 mg/kg). The nitrate liquid did not exhibit an inhibiting effect on the germination ability of seeds. The starting N-methylimidazole used in lower concentrations (1 and 10 mg/kg of soil dry weight) was not phytotoxic, in contrast to higher doses (> 1000 mg/kg).
引用
收藏
页码:1881 / 1892
页数:12
相关论文
共 26 条
[1]   3α-acetoxy-6,6-dimethylbicyclo[3.1.1]heptane-2-spiro-1′-cyclopropane from nopylamine deamination [J].
Abraham, RJ ;
Jones-Parry, R ;
Giddings, RM ;
Guy, J ;
Whittaker, D .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1998, (04) :643-646
[2]   Thermal degradation of ionic liquids at elevated temperatures [J].
Baranyai, KJ ;
Deacon, GB ;
MacFarlane, DR ;
Pringle, JM ;
Scott, JL .
AUSTRALIAN JOURNAL OF CHEMISTRY, 2004, 57 (02) :145-147
[3]   Chiral ionic liquids, a renewal for the chemistry of chiral solvents?: Design, synthesis and applications for chiral recognition and asymmetric synthesis [J].
Baudequin, C ;
Brégeon, D ;
Levillain, J ;
Guillen, F ;
Plaquevent, JC ;
Gaumont, AC .
TETRAHEDRON-ASYMMETRY, 2005, 16 (24) :3921-3945
[4]   Ionic liquids and chirality: opportunities and challenges [J].
Baudequin, C ;
Baudoux, J ;
Levillain, J ;
Cahard, D ;
Gaumont, AC ;
Plaquevent, JC .
TETRAHEDRON-ASYMMETRY, 2003, 14 (20) :3081-3093
[5]   X-RAY STRUCTURE-ANALYSIS OF TOSYLATE ESTER OF (1S,5S)-6,6-DIMETHYL-2-[(2S)-3,3,3-TRICHLORO-2-HYDROXYPROPYL]BICYCLO[3.1.1]HEPT-2-ENE, MAJOR PRODUCT OF IRON(III) CHLORIDE-CATALYZED ENE ADDITION OF CHLORAL TO(-)-(1S,5S)-PIN-2(10)-ENE [J].
BEGLEY, MJ ;
GILL, GB ;
WALLACE, B .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1978, (02) :93-97
[6]   Selective Lewis acid complexation of 2-hydroxyethyl esters using competitive Diels-Alder reactions as a mechanistic probe [J].
Clapham, G ;
Shipman, M .
TETRAHEDRON, 2000, 56 (08) :1127-1134
[7]   New bidentate alkoxy-NHC ligands for enantioselective copper-catalysed conjugate addition [J].
Clavier, H ;
Coutable, L ;
Guillemin, JC ;
Mauduit, M .
TETRAHEDRON-ASYMMETRY, 2005, 16 (05) :921-924
[8]   Studies on the use of surfactants in aqueous Diels-Alder reactions [J].
Diego-Castro, MJ ;
Hailes, HC .
TETRAHEDRON LETTERS, 1998, 39 (15) :2211-2214
[9]   Chiral ionic liquids: Synthesis and applications [J].
Ding, J ;
Armstrong, DW .
CHIRALITY, 2005, 17 (05) :281-292
[10]   Ionic liquid (molten salt) phase organometallic catalysis [J].
Dupont, J ;
de Souza, RF ;
Suarez, PAZ .
CHEMICAL REVIEWS, 2002, 102 (10) :3667-3691