The title compound 7,7-dimethyl-2-amino-3-cyano-4-(3,4-methylene- dioxylphenyl)-5-oxo-5,6,7,8-tetrahydro-4H-benzo-[b]-pyran(C19H18N2O4, Mr=338.35) is mono- clinic, space group C2/c with a=26.753(5), b=9.409(2), c=16.0...The title compound 7,7-dimethyl-2-amino-3-cyano-4-(3,4-methylene- dioxylphenyl)-5-oxo-5,6,7,8-tetrahydro-4H-benzo-[b]-pyran(C19H18N2O4, Mr=338.35) is mono- clinic, space group C2/c with a=26.753(5), b=9.409(2), c=16.036(3)? b=121.00(1), Z=8, V=3460(1)?, Dc=1.299g/cm3, m (MoKa)=0.092mm-1, F(000)=1424, R=0.0410 and wR=0.0926 for 3138 observed reflections (I >2s (I)). X-ray analysis reveals that atoms C(8), C(9), C(10), O(3), C(12) and C(13) form a six-membered ring in which the distances of C(9)-C(10) and C(12)-C(13) are 1.342(2) and 1.331(2) ? respectively, which show that they are C=C double bonds. In addition, there is hydrogen bond in the product molecule.展开更多
The title compound methyl (7,7-dimemyl-2-amino-4-(4-chlorophenyl)-5-oxo-5,6,7,8-tetrahydro-4H-benzo-[b]-pyran-3-yl) carboxylate (C19H20ClNO4, Mr = 361.81) was synthesized and crystallized. The crystal belongs to tricl...The title compound methyl (7,7-dimemyl-2-amino-4-(4-chlorophenyl)-5-oxo-5,6,7,8-tetrahydro-4H-benzo-[b]-pyran-3-yl) carboxylate (C19H20ClNO4, Mr = 361.81) was synthesized and crystallized. The crystal belongs to triclinic, space group P 1 with a = 8.519(2), b = 10.346(2), c = 11.481(3) A, α = 108.16(1), β = 107.78(2), γ= 91.83(2)°, Z = 2, V = 906.5(3) A3, Dc = 1.326 g/cm3, μ(MoKα) = 0.234 mm-1, F(000) = 380, R = 0.0467 and wR = 0.1270 for 3142 observed reflections (I > 2σ(I)). X-ray analysis reveals that the C(7), C(8), C(9), O(1), C(10) and C(11) atoms form a six-membered ring which adopts a boat conformation. In the ring, the distances of C(8)-C(9) and C(10)-C(11) are 1.332(3) and 1.357(3) A, respectively, which indicates that they are C=C double bonds. Another six-membered ring (C(8)-C(9)-C(15)-C(14)-C(13)-C(12)) adopts the half-chair confonnation. In addition, there are intermolecular hydrogen bonds in the crystal structure.展开更多
The oxygenation constants （Ko2） of cobalt（Ⅱ） hydroxamates （CoL^1 2-CoL^3 2） with benzo-15-crown-5 （B15C5） pendants were measured over the range of -5 to ＋20 ℃, and the values of thermodynamic parameters （...The oxygenation constants （Ko2） of cobalt（Ⅱ） hydroxamates （CoL^1 2-CoL^3 2） with benzo-15-crown-5 （B15C5） pendants were measured over the range of -5 to ＋20 ℃, and the values of thermodynamic parameters （ΔH^0 and ΔS^0） were calculated based on these （Ko2） values, Meanwhile, these crowned complexes were employed to the oxidation for p-xylene to p-toluic acid with air at 110Δ under normal atmospheric pressure. The effects of B15C5 pendant and the length of chain bonded to B15C5 in these complexes on the O2-binding capabilities and oxidation for p-xylene were investigated with the comparison of crown-free analogues CoL^4 2.展开更多
A novel Pd(II) Benzo-15-crown-5 complex [Na(B15CS)]_2[Pd(SCN)_4] has been isolated and characterized by IR and X-ray diffraction analysis. The crystal structure belongs to monoclinic, space group P2_1,/n with cell dim...A novel Pd(II) Benzo-15-crown-5 complex [Na(B15CS)]_2[Pd(SCN)_4] has been isolated and characterized by IR and X-ray diffraction analysis. The crystal structure belongs to monoclinic, space group P2_1,/n with cell dimensions, a = l.0164(6), b = l.3743(3), c = l.4987(7) nm, β = 95.248(6) °, V = 2.0847 'nm_3, Z = 2, F(000) = 944, R = 0.053, Rw = 0.072. The compound consists of two [Na(B15CS)]+ complex canons and a [Pd(SCN)4_]^(2-) complex anion. Each sodium ion is coordinated by five crown ether oxygen atoms and one N atom from the SCN group of [Pd(SCN)_4]^(2-) to form stable neutral complex.展开更多
Two novel heteroatom-bridged his (benzo-12-crown-4 ether)s, i.e. his [2-nitro-4,5 (1,4,7,10-tetraoxadecamethylene) disulfide 1 and diselenide 2, have been synthesized. X ray crystallographic structure was obtained for...Two novel heteroatom-bridged his (benzo-12-crown-4 ether)s, i.e. his [2-nitro-4,5 (1,4,7,10-tetraoxadecamethylene) disulfide 1 and diselenide 2, have been synthesized. X ray crystallographic structure was obtained for 1. Ion selective electrodes (ISE) for Ag+, containing 1 and 2 in PVC membrane as neutral carriers, were prepared, and their selectivity coefficients for Ag^+ (K_(Ag.M)^(pot)) were determined against other heavy metal ions, alkali and alkaline-earth metal ions. and ammonium ion. These ISEs showed excellent Ag^+ selectivities, log K_(Ag.M)^(pot) ≤ -3.8, against most of the interfering canons examined, except for Hg^+.展开更多
This paper reports the results on the nature of bond-order and net charge distributions predicted by Ab initio Hartree- Fock procedures for 1-amino-2-iminio-, 1-amino-3-iminio- and 1-amino-4-iminiotropylium cations th...This paper reports the results on the nature of bond-order and net charge distributions predicted by Ab initio Hartree- Fock procedures for 1-amino-2-iminio-, 1-amino-3-iminio- and 1-amino-4-iminiotropylium cations that incorporate, in order, the 1,7-, 1,3- and 1,5-diazapentadienium (vinamidinium) elements. There appears to be very little contribution from tropylium-type charge distribution, the positive charges residing largely in the nitrogen atoms. The partial bond fixations and charge distributions show interesting variation in the three isomers. The 1,3-isomer in which the 1,3-diazapentadienium element is preserved in the favoured zigzag conformation appears to be relatively the best stabilized. The six isomeric benzo-fused derivatives arising from the three amino-iminiotropylium cations show similar differences in patterns of behaviour. Interestingly, the isomer in which a zigzag 1,3-diazapentadienium element is conjugated with a styrene moiety receives the deepest stabilization. While showing that the element largely contributes to the relative stabilization among the systems studied, contribution from certain stereochemical destabilizing factors may not be insignificant.展开更多
A series of tetrahydrobenzo-[b]-pyran derivative was synthesized by the reaction of arylmethylene malononitrile or arylmethylene cyanoacetate with dimedone in ethylene glycol at 80C without catalyst. The structures o...A series of tetrahydrobenzo-[b]-pyran derivative was synthesized by the reaction of arylmethylene malononitrile or arylmethylene cyanoacetate with dimedone in ethylene glycol at 80C without catalyst. The structures of the two products were characterized by X-ray diffraction.展开更多
Two extraction constants (Kex± and Kex) for extraction of silver picrate (Ag﹢Pic﹣) by benzo-15-crown-5 ether (B15C5) and benzo-18-crown-6 one (B18C6) into 1,2-dichloroethane (DCE) and dichloromethane (DCM) were...Two extraction constants (Kex± and Kex) for extraction of silver picrate (Ag﹢Pic﹣) by benzo-15-crown-5 ether (B15C5) and benzo-18-crown-6 one (B18C6) into 1,2-dichloroethane (DCE) and dichloromethane (DCM) were determined at 298 K and given values of ionic strength. Here, Kex± and Kex were expressed as [AgL﹢]o[Pic﹣]o/[Ag﹢][L]o[Pic﹣] and [AgLPic]o/[Ag﹢][L]o[Pic﹣], respectively: L symbolizes B15C5 or B18C6 and the subscript “o” denotes the organic phase composed of DCE or DCM. Individual distribution constants (KD,Pic) of picrate ion, Pic﹣, into the two diluents were also determined with the determination of Kex. From comparison of these KD,Pic values with those standardized, interfacial potential differences () at extraction equilibria were evaluated. Then, using these values, relations of the experimentally-determined logKex± or logKex values with their electrochemically-standardized ones were precisely discussed. Consequently, it was indicated that logKex± should be expressed as a function of .展开更多
基金supported by the Foundation of the Surpassing Project of Jiangsu Province
文摘The title compound 7,7-dimethyl-2-amino-3-cyano-4-(3,4-methylene- dioxylphenyl)-5-oxo-5,6,7,8-tetrahydro-4H-benzo-[b]-pyran(C19H18N2O4, Mr=338.35) is mono- clinic, space group C2/c with a=26.753(5), b=9.409(2), c=16.036(3)? b=121.00(1), Z=8, V=3460(1)?, Dc=1.299g/cm3, m (MoKa)=0.092mm-1, F(000)=1424, R=0.0410 and wR=0.0926 for 3138 observed reflections (I >2s (I)). X-ray analysis reveals that atoms C(8), C(9), C(10), O(3), C(12) and C(13) form a six-membered ring in which the distances of C(9)-C(10) and C(12)-C(13) are 1.342(2) and 1.331(2) ? respectively, which show that they are C=C double bonds. In addition, there is hydrogen bond in the product molecule.
基金This work was supported by the foundation of the "Surpassing Project" of Jiangsu province
文摘The title compound methyl (7,7-dimemyl-2-amino-4-(4-chlorophenyl)-5-oxo-5,6,7,8-tetrahydro-4H-benzo-[b]-pyran-3-yl) carboxylate (C19H20ClNO4, Mr = 361.81) was synthesized and crystallized. The crystal belongs to triclinic, space group P 1 with a = 8.519(2), b = 10.346(2), c = 11.481(3) A, α = 108.16(1), β = 107.78(2), γ= 91.83(2)°, Z = 2, V = 906.5(3) A3, Dc = 1.326 g/cm3, μ(MoKα) = 0.234 mm-1, F(000) = 380, R = 0.0467 and wR = 0.1270 for 3142 observed reflections (I > 2σ(I)). X-ray analysis reveals that the C(7), C(8), C(9), O(1), C(10) and C(11) atoms form a six-membered ring which adopts a boat conformation. In the ring, the distances of C(8)-C(9) and C(10)-C(11) are 1.332(3) and 1.357(3) A, respectively, which indicates that they are C=C double bonds. Another six-membered ring (C(8)-C(9)-C(15)-C(14)-C(13)-C(12)) adopts the half-chair confonnation. In addition, there are intermolecular hydrogen bonds in the crystal structure.
基金The authors gratefully acknowledge the grants from the National Natural Science Foundation of China(No.20072025)Education 0ffice Foundation of Sichuan Province(No.2005C012)Sichuan Provincial Department of Science&Technology(No.2006J13-143)in support of this work.
文摘The oxygenation constants （Ko2） of cobalt（Ⅱ） hydroxamates （CoL^1 2-CoL^3 2） with benzo-15-crown-5 （B15C5） pendants were measured over the range of -5 to ＋20 ℃, and the values of thermodynamic parameters （ΔH^0 and ΔS^0） were calculated based on these （Ko2） values, Meanwhile, these crowned complexes were employed to the oxidation for p-xylene to p-toluic acid with air at 110Δ under normal atmospheric pressure. The effects of B15C5 pendant and the length of chain bonded to B15C5 in these complexes on the O2-binding capabilities and oxidation for p-xylene were investigated with the comparison of crown-free analogues CoL^4 2.
文摘A novel Pd(II) Benzo-15-crown-5 complex [Na(B15CS)]_2[Pd(SCN)_4] has been isolated and characterized by IR and X-ray diffraction analysis. The crystal structure belongs to monoclinic, space group P2_1,/n with cell dimensions, a = l.0164(6), b = l.3743(3), c = l.4987(7) nm, β = 95.248(6) °, V = 2.0847 'nm_3, Z = 2, F(000) = 944, R = 0.053, Rw = 0.072. The compound consists of two [Na(B15CS)]+ complex canons and a [Pd(SCN)4_]^(2-) complex anion. Each sodium ion is coordinated by five crown ether oxygen atoms and one N atom from the SCN group of [Pd(SCN)_4]^(2-) to form stable neutral complex.
文摘Two novel heteroatom-bridged his (benzo-12-crown-4 ether)s, i.e. his [2-nitro-4,5 (1,4,7,10-tetraoxadecamethylene) disulfide 1 and diselenide 2, have been synthesized. X ray crystallographic structure was obtained for 1. Ion selective electrodes (ISE) for Ag+, containing 1 and 2 in PVC membrane as neutral carriers, were prepared, and their selectivity coefficients for Ag^+ (K_(Ag.M)^(pot)) were determined against other heavy metal ions, alkali and alkaline-earth metal ions. and ammonium ion. These ISEs showed excellent Ag^+ selectivities, log K_(Ag.M)^(pot) ≤ -3.8, against most of the interfering canons examined, except for Hg^+.
文摘This paper reports the results on the nature of bond-order and net charge distributions predicted by Ab initio Hartree- Fock procedures for 1-amino-2-iminio-, 1-amino-3-iminio- and 1-amino-4-iminiotropylium cations that incorporate, in order, the 1,7-, 1,3- and 1,5-diazapentadienium (vinamidinium) elements. There appears to be very little contribution from tropylium-type charge distribution, the positive charges residing largely in the nitrogen atoms. The partial bond fixations and charge distributions show interesting variation in the three isomers. The 1,3-isomer in which the 1,3-diazapentadienium element is preserved in the favoured zigzag conformation appears to be relatively the best stabilized. The six isomeric benzo-fused derivatives arising from the three amino-iminiotropylium cations show similar differences in patterns of behaviour. Interestingly, the isomer in which a zigzag 1,3-diazapentadienium element is conjugated with a styrene moiety receives the deepest stabilization. While showing that the element largely contributes to the relative stabilization among the systems studied, contribution from certain stereochemical destabilizing factors may not be insignificant.
文摘A series of tetrahydrobenzo-[b]-pyran derivative was synthesized by the reaction of arylmethylene malononitrile or arylmethylene cyanoacetate with dimedone in ethylene glycol at 80C without catalyst. The structures of the two products were characterized by X-ray diffraction.
基金the National Natural Science Foundation of China (No. 20371040) the Foundation (031-A21-004)of Gansu province and the Foundation (No. 02-18) of Northwest Normal University.
文摘Two extraction constants (Kex± and Kex) for extraction of silver picrate (Ag﹢Pic﹣) by benzo-15-crown-5 ether (B15C5) and benzo-18-crown-6 one (B18C6) into 1,2-dichloroethane (DCE) and dichloromethane (DCM) were determined at 298 K and given values of ionic strength. Here, Kex± and Kex were expressed as [AgL﹢]o[Pic﹣]o/[Ag﹢][L]o[Pic﹣] and [AgLPic]o/[Ag﹢][L]o[Pic﹣], respectively: L symbolizes B15C5 or B18C6 and the subscript “o” denotes the organic phase composed of DCE or DCM. Individual distribution constants (KD,Pic) of picrate ion, Pic﹣, into the two diluents were also determined with the determination of Kex. From comparison of these KD,Pic values with those standardized, interfacial potential differences () at extraction equilibria were evaluated. Then, using these values, relations of the experimentally-determined logKex± or logKex values with their electrochemically-standardized ones were precisely discussed. Consequently, it was indicated that logKex± should be expressed as a function of .
