环氧烷化合物在有机合成中的应用

综述了近年来环氧烷化合物在有机合成中的应用。环氧烷化合物的开环反应可以用来合成其它方法难以合成的多官能团化合物，或通过开环和修饰合成其他环状化合物。另外，利用该反应还可以提供保护基以及立体、区域选择性地合成各种有机化合物。参考文献23篇。     

Liquid-liquid extraction of uranium(VI) with 2-ethylhexyltolylsulfoxide (EHTSO)

The liquid-liquid extraction behavior of 2-ethylhexyltolylsulfoxide (EHTSO) towards uranium(VI) contained in nitric acid aqueous solution has been investigated. It was found that the extraction increases with increasing nitric acid concentration up to 5.0 mol/l and then decreases. Extraction also increases with increasing extractant concentration. The extracted species appears to be UO₂(NO₃)₂ ^.2EHTSO. The influences of temperature, NH₄NO₃ and Na₂C₂O₄ concentrations on the extraction equilibrium were also investigated and the thermodynamic functions of the extraction reaction were obtained.     

Fischer-Tropsch synthesis over cobalt catalysts supported on modified SiO2 with mesoporous silica

SiO₂ was modified by hexagonal mesoporous silica to form a mixture with meso-/macroporous sizes and used as support of Co catalysts for Fischer-Tropsch synthesis in a slurry phase. A synergistic effect on the activity of Co catalyst was found. The catalytic properties are related to the state of surface Co and the character of support.     

邻羟基萘基荧光酮－DDMBA光度法测定微量锗

邻羟基萘基荧光酮－ＤＤＭＢＡ光度法测定微量锗冯永兰，邝代治（衡阳师范专科学校化学系衡阳，４２１００８）关键词：分光光度法，锗，邻羟基萘基荧光酮，溴化十二烷基二甲基苄铵苯基荧光酮类试剂应用于锗的测定已有报导￣［１－６］。但邻羟基萘基荧光酮（β－ＨＮＦ）...     

Bi4PMo(12)O(49)催化剂的性质及其在丙烷选择氧化中的活性

从钼磷酸出发制备了Ｂｉ４ＰＭｏ１２Ｏ４９催化剂，ＩＲ及ＸＲＤ分析结果表明，高温焙烧后其基本组成为α－Ｂｉ２Ｍｏ３Ｏ１２／ＭｏＯ３，考察了该催化剂对丙烷的选择氧化生，ＥＳＲ及ＸＰＳ测定结果表明，反应后催化剂中Ｍｏ＾５＋的含量明显增加，这暗示着反应物种吸附在Ｍｏ＾６＋上，而Ｂｉ则为气相氧的入口。     

β—环糊精对D／L—酪氨酸对映体的手性识别及超分子包合物的合成

利用圆二色谱研究了β－环糊精（β－ＣＤ）对Ｄ／Ｌ酪氨酸的手性识别行为，制备出了β－ＣＤ与Ｌ－酪氨酸（Ｌ－Ｔｙｒ）的固体超分子化合物，并用元素分析、薄层分析、Ｘ射线粉末衍射及热分析对包合物进行了表征，用荧光光谱法测定了包合物的形成常数．实验结果表明，β－ＣＤ具有选择包结Ｌ－酪氨酸的特性；主客体形成１１的包合物，其组成为Ｌ－Ｔｙｒ／β－ＣＤ·１２Ｈ２Ｏ；稳定常数为５．１３×１０３Ｌ／ｍｏｌ；包合物的热稳定性比主客体皆有改善     

Enhanced catalytic reaction at an air–liquid–solid triphase interface

Gaseous reactant involved heterogeneous catalysis is critical to the development of clean energy, environmental management, health monitoring, and chemical synthesis. However, in traditional heterogeneous catalysis with liquid–solid diphase reaction interfaces, the low solubility and slow transport of gaseous reactants strongly restrict the reaction efficiency. In this minireview, we summarize recent advances in tackling these drawbacks by designing catalytic systems with an air–liquid–solid triphase joint interface. At the triphase interface, abundant gaseous reactants can directly transport from the air phase to the reaction centre to overcome the limitations of low solubility and slow transport of the dissolved gas in liquid–solid diphase reaction systems. By constructing a triphase interface, the efficiency and/or selectivity of photocatalytic reactions, enzymatic reactions, and (photo)electrochemical reactions with consumption of gaseous reactants oxygen, carbon dioxide, and nitrogen are significantly improved.

Gaseous reactant involved liquid–solid diphase interface reactions can be significantly enhanced using rationally designed and constructed air–liquid–solid triphase systems.     

A visible-light activated [2 + 2] cycloaddition reaction enables pinpointing carbon–carbon double bonds in lipids

The precise location of C C bonds in bioactive molecules is critical for a deep understanding of the relationship between their structures and biological roles. However, the traditional ultraviolet light-based approaches exhibited great limitations. Here, we discovered a new type of visible-light activated [2 + 2] cycloaddition of carbonyl with C C bonds. We found that carbonyl in anthraquinone showed great reactivities towards C C bonds in lipids to form oxetanes under the irradiation of visible-light. Combined with tandem mass spectrometry, this site-specific dissociation of oxetane enabled precisely locating the C C bonds in various kinds of monounsaturated and polyunsaturated lipids. The proof-of-concept applicability of this new type of [2 + 2] photocycloaddition was validated in the global identification of unsaturated lipids in a complex human serum sample. 86 monounsaturated and polyunsaturated lipids were identified with definitive positions of C C bonds, including phospholipids and fatty acids even with up to 6 C C bonds. This study provides new insights into both the photocycloaddition reactions and the structural lipidomics.

A new visible-light activated [2 + 2] cycloaddition reaction was discovered and enabled pinpointing carbon–carbon double bonds in lipids.     

Cooperatively assembled liquid crystals enable temperature-controlled Förster resonance energy transfer

Balancing the rigidity of a π-conjugated structure for strong emission and the flexibility of liquid crystals for self-assembly is the key to realizing highly emissive liquid crystals (HELCs). Here we show that (1) integrating organization-induced emission into dual molecular cooperatively-assembled liquid crystals, (2) amplifying mesogens, and (3) elongating the spacer linking the emitter and the mesogen create advanced materials with desired thermal–optical properties. Impressively, assembling the fluorescent acceptor Nile red into its host donor designed according to the aforementioned strategies results in a temperature-controlled Förster resonance energy transfer (FRET) system. Indeed, FRET exhibits strong S-curve dependence as temperature sweeps through the liquid crystal phase transformation. Such thermochromic materials, suitable for dynamic thermo-optical sensing and modulation, are anticipated to unlock new and smart approaches for controlling and directing light in stimuli-responsive devices.

A temperature-sensitive Förster resonance energy transfer system was constructed using a highly emissive liquid crystal co-assembled with Nile red, enabling thermo-optical modulation for controlling and directing light in stimuli-responsive devices.     

The Aldol Reaction of Allenolates with Aldehydes in the Presence of Magnesium Diiodide (MgI2) as Catalyst

Stereoselective synthesis of (Z)‐α‐(hydroxyalkyl)‐β‐iodoacrylates (=(2Z)‐2‐(hydroxyalkyl)‐3‐iodoprop‐2‐enoates) was achieved in a one‐pot coupling reaction from methyl prop‐2‐ynoate, Me₃SiI, and an alkanal under mild conditions with MgI₂ as catalyst (→ 1 – 9 ; see Table and Scheme 1). Baylis‐Hillman β‐iodo adducts were generated in excellent yields with high (Z)‐selectivity. The conversion of methyl prop‐2‐ynoate to an active methyl 3‐iodo‐1‐[(trimethylsilyl)oxy]allenolate intermediate in situ followed by carbonyl addition is proposed as the reaction sequence (Schemes 1 and 2).