PubMed Health⌕ Search

Biomedical subjects

Hai-Ying Wang

Publications and source records attributed to Hai-Ying Wang.

4 recordsLinked to original sources

[Molecular mechanism of the decrease in phosphatidylglycerol content in tobacco leaves under phosphate deficiency stress].

Under phosphate deficiency stress, the mRNA levels of PLDalpha and PLDbeta in tobacco older leaves were higher while in rapid developing ones were lower than those in controls. In addition, changes in PG hydrolase activity were positively correlated with the alternation of transcript levels of PLDalpha and PLDbeta genes in both types of leaves. Phosphate deficiency resulted in decreases in PG content in both older and rapid developing leaves, and that the extent of decrease in older leaves was much larger than that in rapid developing ones. Phosphatidic acid (PA) is one of the main hydrolysis product of PG. Its production was restricted by adding n-butanol, an inhibitor of PA formation via PLD pathway, to the in vitro enzyme reaction mixture. These results suggest that the enhanced PG hydrolase activity is one important cause of the decrease in PG content in older leaves, and the activity of PG hydrolase is regulated at the transcriptional level.

1-Butanol↗

Synthesis and characterization of new coordination polymers generated from bent bis(cyanophenyl)oxadiazole ligands and Ag(I) salts.

Two new bent bis(cyanophenyl)oxadiazole ligands, 2,5-bis(4-cyanophenyl)-1,3,4-oxadiazole (L7) and 2,5-bis(3-cyanophenyl)-1,3,4-oxadiazole (L8), were synthesized. The coordination chemistry of these ligands with various Ag(I) salts has been investigated. Seven new coordination polymers, namely, {[Ag(L7)(H2O)]ClO4}n) (1) (triclinic, P1, a = 9.342(4) A, b = 9.889(4) A, c = 10.512(4) A, alpha = 68.978(6) degrees, beta = 78.217(6) degrees, gamma = 81.851(7) degrees, Z = 2), {[Ag(L7)]SO3CF3}n (2) (monoclinic, P2(1)/n, a = 7.559(2) A, b = 23.739(6) A, c = 10.426(3) A, beta = 108.071(4) degrees, Z = 4), {[Ag(L8)]BF4 x 0.5(C6H6) x H2O}n (3) (triclinic, P1, a = 7.498(3) A, b = 10.649(4) A, c = 13.673(5) A, alpha = 98.602(5) degrees, beta = 100.004(5) degrees, gamma =110.232(5) degrees, Z = 2), {[Ag(L8)SbF6] x H2O}n (4) (triclinic, P1, a = 8.2621(9) A, b = 10.6127(12) A, c = 13.3685(15) A, alpha = 98.012(2) degrees, beta = 106.259(2) degrees, gamma = 112.362(2) degrees, Z = 2), {[Ag2(L8)2(SO3CF3)] x H2O}n (5) (triclinic, P1, a = 10.713(4) A, b = 13.449(5) A, c = 15.423(5) A, alpha = 65.908(5) degrees, beta = 74.231(5) degrees, gamma = 83.255(5) degrees, Z = 2), {[Ag2(L8)(C6H6)(ClO4)] x ClO4}n (6) (monoclinic, P2(1)/n, a = 6.9681(17) A, b = 20.627(5) A, c = 17.437(4) A, beta = 95.880(4) degrees, Z = 4), and {[Ag2(L8)(H2PO4)2]}n (7) (triclinic, P1, a = 7.956(2) A, b = 9.938(3) A, c = 14.242(4) A, alpha = 106.191(4) degrees, beta = 97.322(4) degrees, gamma = 107.392(4) degrees, Z = 1), were obtained by the combination of L7 and L8 with Ag(I) salts in a benzene/methylene chloride mixed-solvent system and fully characterized by infrared spectroscopy, elemental analysis, and single-crystal X-ray diffraction. In addition, the luminescence and electrical conductance properties of compounds 1-6 and the host-guest chemistry of compound 3 were investigated.

Journal Article↗

The effects of substitution on tetrakis(substituted imidazole)copper(II) trifluoromethanesulfonates.

The organic ligands 4-methyl-1H-imidazole and 2-ethyl-4-methyl-1H-imidazole react with Cu(CF(3)SO(3))(2).6H(2)O to give tetrakis(5-methyl-1H-imidazole-kappaN(3))copper(II) bis(trifluoromethanesulfonate), [Cu(C(4)H(6)N(2))(4)](CF(3)SO(3))(2), and aquatetrakis(2-ethyl-5-methyl-1H-imidazole-kappaN(3))copper(II) bis(tri fluoromethanesulfonate), [Cu(C(6)H(10)N(2))(4)(H(2)O)](CF(3)SO(3))(2). In the former, the Cu atom has an elongated octahedral coordination environment, with four imidazole rings in equatorial positions and two trifluoromethanesulfonate ions in axial positions. This conformation is similar to those in the analogous complexes tetrakis(imidazole)copper(II) trifluoromethanesulfonate and tetrakis(2-methyl-1H-imidazole)copper(II) trifluoromethanesulfonate. In the second of the title compounds, the ethyl groups block the central Cu atom, and a square-pyramidal coordination environment is formed around the Cu atom, with the substituted imidazole rings in the basal positions and a water molecule in the axial position.

Journal Article↗