Synthesis of Imidazo[2,1‐a]isoquinolines from α‐Tosyloxyketones and 1‐Aminoisoquinoline in Ionic Liquid Solvent

The room temperature ionic liquid n‐butylpyridinium tetrafluoroborate (BPyBF₄) is used as a ‘green’ recyclable alternative to classical molecular solvents for the cyclocondensation of α‐tosyloxyketones with 1‐aminoisoquinoline to prepare imidazo[2,1‐a]isoquinolines in good yields.     

Accuracy, precision and sensitivity in cyclic INAA with short-lived radionuclides

Repeated irradiation enhances the precision and sensitivity of INAA based on short-live radionuclides, but entail systematic losses due to dead time. The relative standard deviation in the net peak area decreases with the square root of the number of cycles while the systematic bias increases with it. The limits of decision, detection and determination decrease in a somewhat more complicated way with the number of cycles. The derived formulation is applied to the determination of selenium in hair by the 161.9 keV photopeak of^77mSe,T _1/2=17.8 s.     

Novel Z-selective head-to-head dimerization of terminal alkynes catalyzed by lanthanide half-metallocene complexes

Various terminal alkynes have been cleanly dimerized into the corresponding head-to-head (Z)-enynes by use of the half-metallocene lutetium alkyl complexes Me2Si(C5Me4)(NAr)Lu(CH2SiMe3)(THF) (Ar = Ph, C6H3Me2-2,6, C6H2Me3-2,4,6) as catalysts. Aromatic C-Cl, C-Br, and C-I bonds, which are known to be extremely susceptible to reductive cleavage by transition metals, survived in the present reactions. The corresponding dimeric alkynide species [Me2Si(C5Me4)(NAr)Lu(mu-CCR)]2 are thought to be the true catalysts, some of which have been isolated and structurally characterized. These alkynide species were thermally stable and soluble at the reaction temperatures (80-110 degrees C), but they precipitated upon cooling to room temperature after completion of the reaction. Therefore, this catalyst system works homogeneously but can be separated and reused, thus constituting the first example of a recyclable catalyst system for the dimerization of terminal alkynes and also the first example of (Z)-selective head-to-head dimerization of aromatic terminal alkynes.     

AQC柱前衍生反相高效液相色谱法测定土壤中氨基酸

以2-氨基丁酸为内标物,6-氨基喹啉基-N-羟基琥珀酰亚氨基甲酸酯(AQC)为柱前衍生试剂,用XTerraC18柱,1.8mmol/L甲酸铵溶液(pH=3.0)和乙腈为流动相,采用梯度洗脱,光电二极管(PDA)检测器在248nm波长处检测,建立了一种利用反相高效液相色谱同时测定土壤中17种氨基酸的分析方法。方法重现性好,精密度高,氨基酸浓度在25~600μmol/L范围内,线性相关系数均大于0.99;各氨基酸检出限≤0.5pmol。并且在该色谱条件下,获得了灵敏度较高,彼此分离良好的17种AQC衍生氨基酸的LC-MS质谱总离子流图,为今后土壤氨基酸的深入研究提供了更加有利的手段。     

同时测定食用植物油中抗氧剂叔丁基对羟基茴香醚和2，6－二叔丁基对甲酚的方法

报道了用高效液用色谱法同时测定食用植物油中的抗氧剂叔丁基对羟基茴香醚（ＢＨＡ）和２，６－二叔丁基对甲酚（ＢＨＴ）的实验方法。采用ＺｏｒｂａｘＯＤＳＣ_（１８）色谱住，甲醇：水（９０：１０，Ｖ／Ｖ）作流动相，检测波长为２４５ｎｍ，流速为１ｍＬ／ｍｉｎ。检测下限分别为１５ｎｇ（ＢＨＡ），９０ｎｇ（ＢＨＴ），回收率分别是９６．８％±９．８％（ＢＨＡ），９９．０％±３．２％（ＢＨＴ）。方法快速、准确，灵敏度高。     

碱解增敏荧光法测定残留甲萘威

甲萘威在0.01mo1/L KOH溶液中可降解为强荧光产物。十六烷基三甲基溴化铵对其增敏后,荧光强度达到其自身荧光强度的6倍。基于此,建立了对残留甲萘威进行荧光测定的新方法。线性动态范围为2.00~1.70×103μg/L;检出限为0.95μg/L;样品的加标回收率在90.2%~99.9%。本法成功地用于叶菜中残留甲萘威的测定。     

The global topological meaning of cocycles in a Gauge group

This Letter shows explicitly that the descent sequence of cocycles in a gauge group realizes the ech-de Rham double complex. Meanwhile the ech complex corresponds to finite gauge transformations. This Letter also shows how the indices of each order of cocycles characterizes the obstructions on overlapping spheres in different dimensions and how these indices are equal to a common one.     

Self-assembly of a series of novel metal-organic compounds containing ferrocenecarboxylate components

Using FcCOONa (Fc = (eta(5)-C(5)H(5))Fe(eta(5)-C(5)H(4))) as starting material, we obtained an unprecedented metal-organic coordination polymer containing ferrocenecarboxylate components [[Pb(2)(FcCOO)(eta(2)-FcCOO)(mu(2)-eta(2)-FcCOO)(mu(3)-eta(2)-FcCOO)(CH(3)OH)].1.5CH(3)OH.H(2)O](n) (1), tetramer [Zn(4)(mu(2)-FcCOO)(6)(mu(4)-O)] (2), and coordination polymers [Pb(FcCOO)(mu(2)-FcCOO)(bpe)](n) (3) (bpe = 1,2-bis(4-pyridyl)ethene), [[Zn(FcCOO)(2)(bpt)].2.5H(2)O](n) (4) (bpt = N,N'-bis(3-pyridylmethyl)thiourea), and [Zn(FcCOO)(eta(2)-FcCOO)(bbp)](n) (5) (bbp = 4,4'-trimethylene-dipyridine). Compounds 1 and 2 are formed by ferrocenecarboxylate units coordinating with Pb(II) or Zn(II). In polymer 1, ferrocenecarboxylate units have four kinds of coordinate modes; just these novel coordinate modes lead to the unprecedented one-dimensional polymer where two kinds of rhomboids are arranged alternatively along the chain. Compound 2 is a tetramer, in which a distinct connectivity of the six ferrocene units is established through the four Zn atoms. Compounds 3-5 are obtained by organic ligands bridging Pb(II) or Zn(II), leading to a new type of metal-organic coordination polymer.     

两个含有平行交替链的新型二氰胺配位高聚物: {Mn(dmpz)[N(CN)2]2}2和{Cu(dmpz)[N(CN)2]2}2

Two new dicyanamide coordination polymers, {Mn(dmpz)[N(CN)2]2}2 (1) and {Cu(dmpz)[N(CN)2]2}2 (2)(dmpz=3,5-dimethylpyrazole), were synthesized and characterized by single crystal X-ray diffraction analysis and IR spectroscopy. In 1 and 2 the metal ions have two different coordination modes, where one is coordinated to four dicyanamide anions and two monodentate dmpz molecules to form a slightly distorted octahedral geometry, while the other adopts octahedral geometry, surrounded by four nitrile N atoms and two amide N atoms of the dicyanamide anions. Both complexes contain two alternating chains that are parallel to each other.     

溶液中芳香单酮的聚集态

本文对九种芳香单酮(苯乙酮、对氯苯乙酮、对甲氧基苯乙酮、对氨基苯乙酮、对硝基苯乙酮、间硝基苯乙酮、2.4-二甲基苯乙酮、1-萘乙酮和1-萘基苯基甲酮)在丙酮溶液中的吸收光谱进行了比较。发现芳香单酮在溶液中的分散是不均匀的, 随浓度增加, 有芳香单酮的聚集体生成。且芳香单酮分子的共轭体系越发达或苯环上电子云密度越犬, 分子就越易聚集。同时提出芳香单酮聚粲时的分子排列是苯环对苯环“面对面”取向的推断。