Preparation of cationic cotton with two-bath pad-bake process and its application in salt-free dyeing

Cationic cotton was prepared by a designed two-bath pad-bake process with 3-chloro-2-hydroxypropyltrimethylammonium chloride as cationizing reagent to realize recycle utilization of the reagent and continuous processing of cationization. Experiments showed that 8.0% (o.w.bath) of the reagent, 1:1 of molar ratio of sodium hydroxide to the reagent, 60 °C and 6 min of baking temperature and time were selected for cationization and the obtained cationic cotton was suitable for application in salt-free reactive dyeing. The structures of both the untreated and cationic fibers were investigated by X-ray diffraction and scanning electronic microscopy. Higher dye utilization and color yields could be realized on the cationic cotton than that on the untreated one in the conventional dyeing. Levelness dyeing and good fastness properties of the dyes on the cationic fabrics were obtained. Besides, colorimetric properties and mechanical strength of the dyed fabrics were both evaluated to show applicability of this preparation process of cationic cotton.     

影响棉纤维分化和发育的因素

影响棉纤维生长发育的主要因素是：基因型、激素、温度、水分、光照、授粉受精状况等。基因型决定棉纤维分化发育方式，内源或外源激素调控纤维分化、伸长、次生壁形成等发育过程。温度对纤维分化发育也有很大程度的影响。离体纤维生长发育除了受上述因素影响外，还受微量元素、维生素、ＮＨ４＾＋、ＣＯ２浓度等影响。     

棉花对大气CO2浓度升高的响应及其对棉蚜种群发生的作用

通过模拟试验研究了棉花对大气 CO2 浓度升高 (70 5 .0 μl/ L 和 10 32 .3μl/ L vs.387.4 μl/ L)的响应及其对棉蚜 (Aphisgossypii Glover)种群发生的作用机制。结果表明 :(1) CO2 浓度升高可以促进棉花的生长 ,显著提高棉花的株高和生物产量 ;(2 )CO2 浓度增加对棉花的光合作用十分有利 ,单株叶面积显著增加 ,同时 ,叶绿素含量也显著增加 ;(3)高的 CO2 浓度可明显影响棉花组织的营养成分和次生代谢物质的含量 ,游离脂肪酸和游离氨基酸显著增加 ,可溶性蛋白含量显著降低 ,此外 ,大气 CO2增加下棉花组织内棉酚和单宁含量也显著增加了 ;(4 )棉蚜的发育历期与棉花组织的游离脂肪酸、游离氨基酸、可溶性蛋白、和棉酚的含量呈显著负相关 ;而棉蚜的繁殖力与组织含水量呈显著负相关 ,与游离脂肪酸、游离氨基酸和棉酚的含量呈显著正相关。大气 CO2 浓度升高主要是通过影响棉花的营养组成和次生代谢物质含量 ,而间接作用于棉蚜 ;未来 ,随着大气 CO2 浓度增加 ,棉花组织营养物质的变化对棉蚜种群的发生和危害有加重的趋势     

赤霉素信号转导与棉纤维的分子发育

赤霉素(Gas)作为一种高效能的植物生长调节物质对棉纤维的分化和发育有着非常重要的影响, 但是, 一直以来有关赤霉素与棉纤维分化和发育的分子机制的研究还很少。文章论述了近年来GA信号组分、转导途径的分子生物学研究进展以及GA与棉纤维分子发育的相关研究成果, 旨在为揭示赤霉素调控棉纤维分化和发育的分子机制以及改善棉纤维品质的棉花育种工作提供新的思路。     

HNO3/H3PO4–NANO2 mediated oxidation of cellulose — preparation and characterization of bioabsorbable oxidized celluloses in high yields and with different levels of oxidation

The reaction of cellulose with a mixture of HNO₃/H₃PO₄–NaNO₂ (2:1:1.4, v/v/%w) at room temperature for different time intervals has been investigated to produce oxidized cellulose (OC), a biocompatible and bioresorbable polymer. The results revealed an increase in carboxyl content of OC with increasing reaction time, corresponding to about 8.0, 13.4, 17.4 and 18.4% carboxyl content after 12, 24, 36, and 48 h, respectively. The yield of OC ranged between 75 and 81%. The use of different ratios of HNO₃ and H₃PO₄, (11:1, 4:1, 2:1, 1:1, 1:2, and 1:4; v/v), in the reaction had no significant effect on the carboxyl content and yield of the OC products. All products, as produced, were low crystallinity (27–35%) fibrous materials. The length of fibers decreased with increasing reaction time. After ball milling for 24 h, the length of fibers further decreased and products converted into a fine powder consisting of small fibers and aggregated non-fibrous particles. The degrees of polymerization (DP) of the OC products produced after 12, 24, and 48 h of reaction duration were 81, 63, and 53, respectively. After ball milling for 24 h, the corresponding values changed to 57, 51 and 46. However, no significant change in the crystallinity of the products was noted after ball milling. The TGA results showed the OC products to be less thermally stable than cellulose. The degradation temperature appears to decrease with increasing carboxyl content. In conclusion, the results show that the low crystallinity OC products can be successfully prepared in high yields and with different levels of carboxyl content from cellulose by treatment with a mixture of HNO₃/H₃PO₄–NaNO₂.     

A seven-coordinate Fe compound: [Fe{O(CH2CO2)2}(H2O)2(NO3)]. Preparation, structure and magnetic properties

A seven-coordinate Fe^III complex, [Fe(oda)(H₂O)₂(NO₃)], was obtained after dissolving Fe(NO₃)₃ · 9H₂O in an aqueous solution of oxydiacetic acid (H₂oda) at room temperature. In the solid state, the Fe^III center adopts a pentagonal bipyramid geometry with an {FeO₇} core formed by a tridentate oda²⁻ and a bidentate in the equatorial plane, and two axial water molecules. Magnetic measurements and EPR spectra revealed the presence of S = 5/2 Fe^III centers with rhombic zero field splitting parameters (D = 0.81 cm⁻¹, E/D = 0.33 ). Weak antiferromagnetic interactions with J ≈ −0.06 cm⁻¹ operating between neighboring Fe ions connected through Fe-O-C-O?H-O-Fe paths are estimated using the molecular field approximation.     

Preparation and biochemical properties of PGH3

PGH₃ was biosynthesised from all-cis-5,8,11,14,17-eicosapentaenoic acid (20:5ω3) by an acetone-pentane powder of ram seminal vesicles and its structure was confirmed by GLC-MS after its reduction to PGF₃α. PGH₃ was transformed by horse platelet microsomes to TXB₃, and by aortic microsomes to Δ¹⁷-6-keto-PGF₁α. The structures of these compounds were confirmed by GLC-MS.     

Synthesis, crystal structure and magnetic properties of a chain coordination polymer {[Cu4L2(H2O)] · H2O}n

A chain coordination polymer with the chemical formula {[Cu₄L₂(H₂O)] · H₂O}_n, has been synthesized by the assembly reaction of K₂CuL · 1.5H₂O and Cu(OAC)₂ · H₂O with a 1:1 mole ratio in methanol, where H₄L = 2-hydroxy-3-[(E)-({2-[(2-hydroxybenzoyl)imino]ethyl}imino)methyl] benzoic acid, OAC⁻ = CH₃COO⁻. The crystal structure was determined by single-crystal X-ray diffraction analysis, the compound has chain molecular structure formed by dissymmetrical tetranuclear units. The magnetic measurements showed that Cu-Cu of the complex exhibit antiferromagnetic interactions, and satisfactory fittings to the observed magnetic susceptibility data were obtained by assuming a binuclear system, and further using molecular field approximation to deal with magnetic exchange interactions between binuclear systems.     

Synthesis, structure and properties of TTF-carboxylate bridged paddlewheel dirhodium complexes, Rh2(BuCO2)3(TTFCO2) and Rh2(BuCO2)2(TTFCO2)2

Reaction of tetrathiafulvalene carboxylic acid (TTFCO₂H) with paddlewheel dirhodium complex Rh₂(Bu^tCO₂)₄ yielded TTFCO₂-bridged complexes Rh₂(Bu^tCO₂)₃(TTFCO₂) (1) and cis- and trans-Rh₂(Bu^tCO₂)₂(TTFCO₂)₂ (cis- and trans-2). Their triethylamine adducts [1(NEt₃)₂] and cis-[2(NEt₃)₂] were purified and isolated with chromatographic separation, and characterized with single crystal X-ray analysis. Trans-[2(NEt₃)₂] is not completely separated from a mixture of cis- and trans-[2(NEt₃)₂], but its single crystals were obtained from a solution of the mixture. A three-step quasi-reversible oxidation process was observed for 1 in MeCN. The first two steps correspond to the oxidation of the TTFCO₂ moiety and the last one is the oxidation of the Rh₂ core. The oxidation of cis-2 is observed as a two-step process with very similar E_1/2 values to those of the first two processes for 1. Both 1⁺ and cis-2²⁺ in MeCN at room temperature show isotropic ESR spectra with a g value of 2.008 and a_H = 0.135 mT for two equivalent H atoms and a_H = 0.068 mT for one H atom. The redox and ESR data of cis-2 suggest that the intramolecular interaction between the TTF moieties is very small.     

Preparation and properties of an o-diphenol: O2 oxidoreductase from cocoa husk

A particulate preparation from cocoa husk which shows o-diphenol: O₂, oxidoreductase activity contains a copper protein moiety linked to a partially formed insoluble polyphenol polymer. The particles are easily stained with osmium tetroxide for electron microscopy and show marked o-diphenol-polymerisation properties when incubated with substrate. The activity and kinetic parameters of the particles against a number of substrates and inhibitors have been determined.     

Designing and transgenic expression of melanin gene in tobacco trichome and cotton fiber

In Streptomyces antibioticus, there are two genes TYRA and ORF438 required for the melanin biogenesis. To investigate whether expression of these two genes in cotton can change cotton fiber colour, we modified the TYRA and ORF438 genes to make their codon usage closer to the codon preference of cotton fiber genes. The resulting versions of these two genes were referred to as DTYRA and DORF438, respectively. Vacuolar targeting signals were also added to their ends. Under the cotton fiber specific LTP3 promoter, DORF438 and DTYRA were first transformed into model plant tobacco (Nicotiana tabacum). Molecular analyses showed that both the DORF438 and DTYRA genes were successfully expressed in transgenic plants, and the melanin deposition was observed in the trichomes of transgenic tobacco. Excitedly, when the same DORF438 and DTYRA expression cassettes were transformed into cotton (Gossypium hirsutum L.) by pollen tube pathway, the colour of cotton fiber changed from white to brown. Molecular analyses confirmed that both genes were transformed into cotton and expressed successfully. All these results indicate that the synthesized DOFR438 and DTYRA genes can work well in tobacco and cotton. Our study may provide a potential method for modifying the colour of cotton fiber.     

Response of the enzymes to nitrogen applications in cotton fiber (Gossypium hirsutum L.) and their relationships with fiber strength

To investigate the response of key enzymes to nitrogen (N) rates in cotton fiber and its relationship with fiber strength, experiments were conducted in 2005 and 2006 with cotton cultivars in Nanjing. Three N rates 0, 240 and 480 kgN/hm2, signifying optimum and excessive nitrogen application levels were applied.The activities and the gene expressions of the key enzymes were affected by N, and the characteristics of cellulose accumulation and fiber strength changed as the N rate varied. Beta-1,3-glucanase activity in cotton fiber declined from 9 DPA till boll opening, and the beta-1, 3-glucanase coding gene expression also followed a unimodal curve in 12—24 DPA. In 240 kgN/hm² condition, the characteristics of enzyme activity and gene expression manner for sucrose synthase and beta-1,3-glucanase in developing cotton fiber were more favorable for forming a longer and more steady cellulose accumulation process, and for high strength fiber development.     

Crystal structures of MoCl2(O)(O2)(OPMePh2)2 and mixtures of MoCl2(O2)(OPPh3)2 and MoCl2(O)(O2)(OPPh3)2: allylic alcohol isomerization studies using MoCl2(O)(O2)(OPMePh2)2

Adding one equivalent of H₂O₂ to compounds of stoichiometry MoCl₂(O)₂(OPR₃)₂, OPR₃ = OPMePh₂ or OPPh₃, leads to the formation of oxo-peroxo compounds MoCl₂(O)(O₂)(OPR₃)₂. The compound MoCl₂(O)(O₂)(OPMePh₂)₂ crystallized with an unequal disorder, 63%:37%, between the oxo and peroxo ligands, as verified by single-crystal X-ray diffractometry, and can be isolated in reasonable yields. MoCl₂(O)(O₂)(OPPh₃)₂, was not isolated in pure form, co-crystallized with MoCl₂(O)₂(OPPh₃)₂ in two ratios, 18%:82% and 12%:88%, respectively, and did not contain any disorder in the arrangement of the oxo and peroxo groups. These complexes accomplish the isomerization of various allylic alcohols. A mechanism of this reaction has been constructed based on ¹⁸O isotopic studies and involves exchange between the alcohol and metal bonded O atoms.     

Association analysis of fiber quality traits and exploration of elite alleles in Upland cotton cultivars/accessions （Gossypium hirsutum L.）

Exploring the elite al eles and germplasm acces-sions related to fiber quality traits wil accelerate the breeding of cotton for fiber quality improvement. In this study, 99 Gossypium hirsutum L. accessions with diverse origins were used to perform association analysis of fiber quality traits using 97 polymorphic microsatel ite marker primer pairs. A total of 107 significant marker-trait associations were detected for three fiber quality traits under three different environments, with 70 detected in two or three environments and 37 detected in only one environment. Among the 70 significant marker-trait associations, 52.86% were reported previously, implying that these are stable loci for target traits. Furthermore, we detected a large number of elite al eles associated simulta-neously with two or three traits. These elite al eles were mainly from accessions col ected in China, introduced to China from the United States, or rare al eles with a frequency of less than＆amp;nbsp;5%. No one cultivar contained more than half of the elite al eles, but 10 accessions were col ected from China and the two introduced from the United States did contain more than half of these al eles. Therefore, there is great potential for mining elite al eles from germplasm accessions for use in fiber quality improvement in modern cotton breeding.     

Novel long bipyridine-type linking ligands containing an intervening naphthalene fragment: [Zn(L)(NO3)2], [Zn(L)(NO3)2], and [Cd(L)1.5(NO3)2] (L = (4-py)-CHN-C10H6-NCH-(4-py); L = (3-py)-CHN-C10H6-NCH-(3-py))

Novel bipyridine-type linking ligands L¹ ((4-py)-CHN-C₁₀H₆-NCH-(4-py)) and L² ((3-py)-CHN-C₁₀H₆-NCH-(3-py)), a pair of isomers due to possessing different pairs of terminal pyridyl groups, were prepared by the Schiff-base condensation. In ligand L¹, the N?N separation between the terminal pyridyl groups is 16.0 Å, with their nitrogen donor atoms at the para positions (4,4′). The corresponding N?N separation in ligand L² is 14.2 Å, with the nitrogen donor atoms at the meta positions (3,3′). 1-D zigzag-chain coordination polymers [Zn(L¹)(NO₃)₂] (1) and [Zn(L²)(NO₃)₂] (2) were prepared by reactions of Zn(NO₃)₂ · 6H₂O with ligands L¹ and L², respectively, by solution diffusion. Polymer 3, [Cd(L¹)_1.5(NO₃)₂], prepared from Cd(NO₃)₂ · 4H₂O and L¹, exhibits a 1-D ladder structure, whose repeating ladder unit consists of four Cd metals and four L¹ ligands to create a large 76-membered ring with dimensions of 20.8 × 20.8 Å. All products were structurally characterized by X-ray diffraction.     

A 2-D polymer assembled by cubane-like clusters [Tb4(OH)4(phen)3(H2O)3] and 3-sulfobenzoate

A coordination polymer {[Tb₄(3-SBA)₄(OH)₄(phen)₃(H₂O)₃] · 7H₂O}_n (3-SBA = 3-sulfobenzoate, phen = 1,10-phenanthroline) was synthesized and structurally characterized. The complex contains cubane-like clusters, [Tb₄(μ₃-OH)₄(phen)₃(H₂O)₃]⁸⁺, which are further linked through 3-SBA ligands to form a 2-D grid-like network structure with topology of (3³, 4⁴, 5³). The complex exhibits strong photoluminescence of the Tb³⁺ ion.