氟

RESULTS: All aromatic anesthetics inhibited I at a holding potential which produce half-maximal current V(1/2; inhibition was modest with 1,3,5-trifluorobenzene (8%+/- 2%), pentafluorobenzene (13%+/- 2%), and hexafluorobenzene (13%+/- 2%), but greater with benzene (37%+/- 2%), fluorobenzene (39%+/- 2%), 1,2-difluorobenzene (48%+/- 2%), 1,4-difluorobenzene (31 +/- 3%), and 1,2,4-trifluorobenzene (33%+/- 1%).

结果：在最高电流的一半的控制电压下所有芳香族麻醉药都阻断钠电流；均苯三酚（8%+/- 2%）、戊苯(13%+/- 2%)、戌苯(13%+/- 2%)的抑制是适度的比苯(37%+/- 2%)、氟苯(39%+/- 2%)，1.2-二氟二苯(48%+/- 2%)，1，4-二氟二苯(31 +/- 3%)，和1，2，4三氟苯(33%+/- 1%)明显。

Glioma is still one of refractory disease in the neurosurgical field; the development of new primary and adjuvant treatment is vital. Recently, the gene therapy of glioma is developed rapidly and there are many methods about the gene therapy that include: suicide gene therapy, immunologic gene therapy, drug resistangce gene therapy, angiostatin gene therapy and so on. The sucide gene therapy is the most potential approach of antitumer, these nonmammalian genes encode enzyme that convert nontoxic prodrugs into highly toxic metablites. Cells transfected with suicide genes are targeted for specific negative selection, witch can be induced by administrtion of the corresponding produg. Among the enzyme/produg combinations, two of the best characterized system are herpes simplex virus thymidine kinase /ganciclovir and Escherichia coli cytosine deaminase /5-flourocytosine (5-FC). The formor can convert the antiviral nucleoside analogs acyclovir , ganciclovir to their nucleoside monophosphate derivatives, the monophosphate forms are subsequently phosphorylated by endogenus cellular kinases to triphosphates, these molecules are potent inhibitors of DNA synthesis.

近年来脑胶质瘤的基因治疗发展迅速，应运而生的方法有自杀基因、免疫基因、多药耐药基因以及抗血管生成基因等，其中自杀基因被认为是最有前景的基因治疗方法，它又称病毒介导的酶／药物前体疗法，是利用转基因技术将哺乳动物细胞中所不含有的自杀基因转入到哺乳动物肿瘤细胞中，该基因表达的产物可将无毒的药物前体转化为毒性药物，从而选择性杀伤该肿瘤细胞，常用的自杀基因有单纯疱疹病毒-胸苷激酶基因和大肠杆菌胞嘧啶脱氨酶基因，前者催化无毒性抗病毒核苷类似物如丙氧鸟苷、无环鸟苷等成为单磷酸核苷衍生物，然后在内源性细胞激酶作用下转化为具有明显毒性的三磷酸核苷，作为DNA合成链的终止剂和DNA合成酶的抑制剂，干扰细胞DNA的合成；后者编码的胞嘧啶脱氨酶可催化5-氟胞嘧啶（5-FC）脱氨成为5-氟尿嘧啶（5-FU），然后代谢为有毒性的5-氟尿嘧啶-5′三磷酸（5-FUTP）和5-氟-2′脱氧尿嘧啶-5′磷酸（5-FdUTP），5-FUTP通过与UTP竞争性结合而抑制mRNA和tRNA的合成，5-FdUTP则作用于胸苷合成酶，导致TMP衰竭而阻止DNA的合成，最终诱导肿瘤细胞凋亡。

Polyvinylidene fluoride is polymer of VDF and few TFE.

聚偏氟乙烯是由偏氟乙烯和少量四氟乙烯共聚制得的氟聚合物。

Study of PES-PAN blending membrane ;2. The blending membrane s of perfluorinated sulfonic resin with polyvinylidene fluoride were prepared by the method of solution casting.

为了降低质子交换膜的成本，选用聚偏氟乙烯和全氟磺酸树脂为原料，采用溶液-浇铸法制备了全氟磺酸树脂/聚偏氟乙烯的共混膜。

Methods A set of demineralized bovine teeth specimens we re measured for microhardness to assess the degree of remineralization,and other two sets of bovine teeth specimens were examined with polarizing microscope to assess the anti-demineralization and anti-caries effect.

利用显微硬度计测定氟化牛奶和氟水对早期人工龋的再矿化作用。利用偏光显微镜观察氟化牛奶和氟水的抗酸脱矿作用及抗龋作用。

In the process, 2, 4-difluoroaniline is used to carry out ammoniated reaction. Then through a series of similar reactions, the important intermediate of temafloxacin, which is called 7-chloro-6-fluoro-1-(2, 4-difluorophenyl)-1, 4-dihydro-4-oxo-3-quinoline acid, is gained.

与环丙沙星和二氟沙星类似，用2，4-二氟苯胺进行胺化反应，再进行一系列类似的反应，制得合成替马沙星的关键中间体7-氯-6-氟-1-（2，4-二氟苯基）-1，4-二氢-4-氧代喹啉-3-羧酸。

The influence of CFC-12 content, effect of fluorination temperature and fluorinating time on the structure and hydrodesulfurization activity of the catalysts were examined systematically. The results revealed that hydrodesulfurization activity of the catalyst fluorinated by 1% CFC-12 at 623 K was obviously improved With an increase of 20%-30% as compared With that of the unfluorinated catalyst, the commercially available BY2 catalyst, and NH4F-fluorinated catalysts.

通过对0.5%~7%各种氟里昂浓度和473~773K各种温度及不同时间氟化处理的样品进行详细考察，发现在623K下由含氟里昂1%的湿空气氟化的载体制备的催化剂样品，其噻吩的加氢脱硫的活性有明显改善，相对於非氟化样品、BY-2工业催化剂以及氟化铵溶液浸渍处理的催化剂活性提高20%~30%，且非常稳定。

Lithium perfluoroalkylphosphonate was synthesized by LiF and perfluoroalkylphosphonate acid obtained by electrochemically fluorinating chlorodiisopropylphosphine. Some properties of a kind of electrolyte that was made from dissolving the lithium perfluoroalkylphosphonate in the mixed solvent with ethylene carbonate and dimethyl carbonate mass ratio 1∶1 were investigated, such as conductivity, stability toward hydrolysis and oxidative decomposition potential, and so on.

选取氯代二异丙基膦(C6H14PCl)为原料，利用电化学氟化方法，得到全氟烷基膦酸[(C3F7)2PF3]，(C3F7)2PF3与氟化锂反应得到全氟烷基膦酸锂Li[(C3F72PF4]，将其溶于碳酸乙烯酯和碳酸二甲酯质量比为1∶1的混合溶剂中得到电解液，考察电解液的电导率、抗水性及氧化分解电位。

Chiral nonracemic fluoro-organic molecules with a fluorine atom on a stereogenic center are readily prepared via chiral electrophilic fluorinating reagent-mediated enantioselective fluorinations, substrate-controlled enantioselective electrophilic fluorinations, chiral metal complexes and asymmetric catalyst—directed catalytic enantioselective fluorinations.

高光学活性的手性氟化物可通过手性亲电氟化试剂诱导的立体选择性氟化反应，基于底物的手性氟化反应以及手性催化剂诱导的不对称催化氟化反应等来制备。

According to the change of the kinds of elements content in slag, F in slag volatilizes in the form of KF and NaF, KF volatilizes much more easily than NaF, KF plays a leading role in the F volatilization, theoretical analysis shows that the saturation vapour pressure of KF in the test slag is 31. 4 times of NaF; when F content is far more than K, KF volatilization is first order grade reaction, it is dominated by K content, the apparent activate energy is 275. 30KJ/mol.

4依据对含氟熔渣中高温条件下（1450℃、1505℃）的各种元素含量的变化情况，发现氟在熔渣中是以碱金属氟化物挥发，并且，KF比NaF具有更好的挥发性，在氟的挥发中占主导地位，理论研究也证明，在1505℃试验组成的熔渣中，KF的饱和蒸气压是NaF的31.4倍；在含氟量远大于钾含量的情况下，KF挥发为一级反应，受钾浓度控制，其表观活化能为275.30KJ／mol。

The labia have now been sutured together almost completely.The drains and the Foley catheter come out at the top.

此刻阴唇已经几乎完全的缝在一起了，排除多余淤血体液的管子和Foley导管从顶端冒出来。

To get the business done, I suggest we split the difference in price.

为了做成这笔生意，我建议我们在价格上大家各让一半。