毛细管气相色谱法测定牛奶中有机氯和有机磷农药残留量

采用一个较快速、简单的方法测定牛血中有机氯和有机磷农药残留物。牛奶中农残经氯仿萃取和固相提取净化后，分别用气相色谱－电子捕获检测器和气相色谱－火焰光度检测器直接测定，色谱柱为ＨＰ－１接ＨＰ－５、ＤＢ１７大口径石英毛细管柱。本法对１７种有机氯农残的回收效率范围为７１．２％￣９９．７％，检测限为０．５￣９μｇ／ｋｇ。而１１种有机磷农残的回收率范围为７０．１％￣９６．１％，检测限则为０．０１￣０．０４ｍ     

用气相色谱法测定粮谷和油籽中氯苯胺灵残留量

确立了粮谷和油籽中氯苯胺灵残留量的气相色谱测定方法，试样采用甲醇提取，经与正己烷液液分配，再以弗罗里硅土柱净化，毛细管柱气相色谱－氮磷检测器测定。方法简便、准确、检出限０．０２μｇ／ｇ，添加回收率为８７．５－９２．９％，相对标准偏差为３．５－７．０％。     

坚果及其制品中匹克司残留量气相色谱测定法

确立了坚果及其制品中匹克司残留量的气相色谱测定方法试样采用甲醇提取，经ＰＴ－硅镁柱净化，ＧＣ－ＥＣＤ测定，方法简便，快速灵敏，检出限０．０２＊１０＾－３ｇ／ｋｇ，添加回收率８７．４％－９３．２％，相对标准偏差４．４％－６．８８％．。     

用大口径毛细管柱气相色谱法测定蜂蜜中杀虫脒残留量

蜂蜜中杀虫脒残留量用气相色谱－氮磷检测器（ＧＣ－ＮＰＤ）直接测定，色谱柱为ＨＰ－５大口径毛细管柱，方法的回收率为７８．３％～９２．５％，变异系数为４．２％，最低检测限２×１０－９。样品前处理采用了微量化学法。     

气相色谱—原子发射光谱法测定水中微量路易氏剂的水解产物

本文用气相色谱－微波诱导等离子体原子发射光谱检测器（ＧＣ－ＭＩＰ－ＡＥＤ）对水中微量路易氏剂的水解产物的测定方法进行了研究，在酸性条件下，路易氏剂的水解产物与２，３－二巯基丙醇（ＢＡＬ）迅速反应形成挥发性的衍生物，在４８０．１９２，１８１．３７９和１８９．０４２ｎｍ波长下分别检测了衍生物的氯，硫，砷元素的发射信号，最小检测量为０．１μｇ／Ｌ。回收率为８７．２％～９７．４％。     

气相色谱／氢火焰检测器检测HL—60细胞DNA中氧化损伤产物8—羟基鸟嘌呤的

用０．４ｍｍｏｌ／ＬＨ２Ｏ２处理ＨＬ－６０细胞株２４ｈ,采用气相色谱／氢火焰检测器检测ＤＮＡ氧化损伤产物８－羟基鸟嘌呤,并用气相色谱－质谱仪选择性离子检测对其进一步鉴定。所用方法的平均回收率为８１．７％,ＲＳＤ小于５％。     

氢化物－气相色谱的元素光度检测器

研究开发的一种新型的元素光度检测器主要用于锗、砷、锡和锑的氢化物气相色谱检测，具有高灵敏，高选择性。它是在普通火焰光度检测器的基础上加装了特制的滤光片改制而成的。对锗、砷、锡和锑的检测限分别为３．０×１０￣（－１１）ｇ、７．０×１０￣（－１１）ｇ、７．０×１０￣（－１０）ｇ和１．１×１０￣（－８）ｇ，相对标准偏差分别为１．８％、２．４％、２．６％和３．０％。     

氢化物－气相色谱的元素光度检测器

 研究开发的一种新型的元素光度检测器主要用于锗、砷、锡和锑的氢化物气相色谱检测，具有高灵敏，高选择性。它是在普通火焰光度检测器的基础上加装了特制的滤光片改制而成的。对锗、砷、锡和锑的检测限分别为３．０×１０￣（－１１）ｇ、７．０×１０￣（－１１）ｇ、７．０×１０￣（－１０）ｇ和１．１×１０￣（－８）ｇ，相对标准偏差分别为１．８％、２．４％、２．６％和３．０％。     

土壤中绿黄隆残留量分析方法的研究

本文确立了土壤中绿黄隆残留量的间接气相色谱分析方法，用０．１５ｍｏｌ／Ｌ ＮａＨＣＯ３提取土样，二氯甲烷洗涤初步纯化后，在水浴上加热水解，再用二氯甲烷萃取，弗罗里硅土柱净化，最后用气相色谱－电子捕获检测器检测水解产物邻氯苯磺酰胺。土壤中添加回收率７８．５％－９０．８％，检测极限０．３ｎｇ／ｇ。     

衍生化气相色谱－质谱法测定水中的路易氏剂及砷酸

本文研究了用气相色谱－质谱法测定水中微量路易氏剂及砷。在酸性条件下，路易氏剂及水解产物２，３－二巯基丙醇迅速反应形成挥发性的衍生物，大大提高了测定灵敏度。用选择性离子检测定量，最小检测量为每升水中１μｇ。路易氏剂的加标回收率为９５．６２％～１０５．８８％之间，砷的加标回收率为９６．３５％～１０６．０３％之间。     

二氧化碳和丙烯直接合成甲基丙烯酸的NiPMo/TiO2催化剂的研究

用溶胶-凝胶法以磷钼酸(MPA)的镍盐溶液水解钛酸四丁酯制备了NiPMo/TiO2催化剂.使用ICP、 XRD、 TG-DTA、 IR、 TPD-MS和微反应技术研究了催化剂的化学组成、热稳定性、化学吸附性质和催化反应性能.杂多钼酸盐与TiO2通过O2-在TiO2表面发生了键合.在623 K下,杂多阴离子仍保持原有的Keggin结构.CO2在Lewis酸位Ni(Ⅱ)和Lewis碱位Ni-O-Mo的桥氧协同作用下生成CO2卧式吸附态Ni(Ⅱ)←O-(CO)←(O--Ni).丙烯有多种吸附态在催化剂上吸附.在563 K、 1 MPa和空速1500 h-1的反应条件下,丙烯的摩尔转化率为3.2%,产物MAA选择性为95%.     

Toward new camptothecins. Part 6: Synthesis of crucial ketones and their use in Friedländer reaction

In the context of the preparation of camptothecin and luotonin A analogs, the synthesis of some key keto-precursors and their use in Friedländer condensation are described. This paper also focuses on the stability of these keto intermediates and emphasizes the major differences between indolizinones and pyrroloquinazolinones series. Noteworthy is also the report of some original structures isolated as by-products of some experiments.     

CoFe2O4自形成磁性液体场致结构化对磁化的影响

The Langevin paramagnetic theory can’t describe the relation between magnetization of ferrofluids and applied magnetic field. The structuralization of ferrofluids, which is considered the main influence factor of the magnetization, is regarded. The part of magnetization works is deposited when the structure is forming. This action influences the magnetization of ferrofluids directly or indirectly. On the base of the “compressing” model, the Langevin function that usually describes the magnetization of ferrofluid is modified, and a well-fitted curve is obtained. An equation of the relation between the equivalent volume fraction after being “compressed” and the intensity of magnetic field is discovered, which approximately describes the process of magnetization. The relation between the approximate initial susceptibility and the volume fraction can be obtained from modified formula.     

Highly regioselective Buchwald–Hartwig amination at C-2 of 2,4-dichloropyridine enabling a novel approach to 2,4-bisanilinopyridine (BAPyd) libraries

The highly regioselective Buchwald–Hartwig amination at C-2 of the cheap and readily accessible reagent, 2,4-dichloropyridine with a range of anilines and heterocyclic amines is described. This new methodology is robust and provides a facile access to 4-chloro-N-phenylpyridin-2-amines on 0.25 mol scale. These intermediates undergo a further Buchwald–Hartwig amination at higher temperature to enable rapid exploration of the chemical space at C-4 and to provide a library of 2,4-bisaminopyridines.     

KMnO4-mediated oxidative CN bond cleavage of tertiary amines: Synthesis of amides and sulfonamides

KMnO₄-mediated oxidative CN bond cleavage of tertiary amines producing secondary amine was introduced, which was trapped by electrophiles (acyl chloride and sulfonyl chloride) to form amides and sulfonamides. The reaction could take place at mild condition, tolerating a wide range of function groups and affording products in moderate to excellent yields.     

Chemistry of heterocyclic compounds at the A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, over 50 years (Review)

The review contains a concise historical account and information on the most significant researches undertaken by the staff at the A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences on the Chemistry of Heterocyclic Compounds. Dedicated to Academician of the Russian Academy of Sciences B. A. Trofimov on his 70th jubilee. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1443–1502, October, 2008.     

Sulfur-directed metal-free and regiospecific methyl C(sp3)–H imidation of thioanisoles

Regiospecific and direct imidation of the methyl C(sp³)–H bond of thioanisoles is realized under mild and metal-free conditions with N-fluorobis(benzenesulfonyl)imide as an oxidant and nitrogen source. Proposed mechanism suggests that thionium ion intermediates and a Pummerer-type reaction are involved. The imidation has advantages such as high step-economy, excellent functionality tolerance, and regiospecificity, giving structurally diverse imidation products.     

Selective syntheses of 2H-1,3-oxazines and 1H-pyrrol-3(2H)-ones via temperature-dependent Rh(II)-carbenoid-mediated 2H-azirine-ring expansion

The Rh(II)-catalyzed reaction of 2-carbonyl-substituted 2H-azirines with ethyl 2-cyano-2-diazoacetate or 2-diazo-3,3,3-trifluoropropionate provides an easy access to 2H-1,3-oxazines and 1H-pyrrol-3(2H)-ones. These compounds can be selectively prepared from the same starting material using temperature as the only varied parameter. The 2-azabuta-1,3-diene intermediate, a common precursor for both heterocyclic products, isomerizes into 2H-1,3-oxazine under kinetic control, while 1H-pyrrol-3(2H)-one is the sole product of the reaction at elevated temperatures. According to DFT-calculations a one-atom oxazine ring contraction involving ring-opening to a 2-azabuta-1,3-diene intermediate, followed by a 1,5- and 1,2-prototropic shift leads to the consecutive formation of imidoylketene and azomethine ylide, which then further undergo cyclization to the pyrrole derivative.     

Synthesis of 1-benzyloxypyrazin-2(1H)-one derivatives

Different approaches for the synthesis of 1-benzyloxypyrazin-2(1H)-one derivatives from simple amino acids have been investigated. A library of 33 precursors for the preparation of N-hydroxy pyrazinones was obtained in moderate to good yields.