高血压症与微量元素

临床上将高血压分为原发性和继发性两类。原发性高血压称为高血压病。高血压症分为3型,即缓进型、急进型和老年性高血压。老年性高血压又称收缩性高血压,其特征是收缩压升高,舒张压变化很小,脉压增大,常合并冠心病。高血压症与微量元素锶、锌、铜有关。国内研究发现,人体内锶(Sr)含量愈低,则血压愈高。一期、二期、三期高血压患者的锶含量分别为5·26×10-3、2·77×10-3和1·65×10-3。国外学者观察46例妊娠高血压患者,其锌、铜、硒、铁、钙、镁及维生素E缺乏。但也有报道指出,高血压患者头发铜及血清铜升高。作者认为,出现这两种截然不同的结果是可以理解的。情况可能无变化,缺锌易患高血压,但早期缺锌者其血铜可能无变化,因锌与铜相拮抗,长期或严重缺锌会导致血铜升高。高血压患者应补充钾、锶、锌和硒。有遗传性钠过敏史者,高钠摄入、高钠潴留是导致高血压的危险因素。钠、钾相拮抗,因此补钾可减少体内钠的潴留。水果和蔬菜是富钾食物。服用药物碘化钾或碘酸钾应有医师指导。海带中锶含量相当高,是理想的补锶食品。核桃、花生、芝麻和瘦肉富锌。服用硒锌氨基酸口服液既可补锌又能补硒,对改善临床症状效果明显。此外,减少患者体内的铅、镉负荷有利于...     

庆祝游效曾院士80华诞暨教学研究60周年

<正>2013年是我国著名无机化学家、中国科学院院士游效曾先生80华诞。游效曾先生,1934年生。武汉大学学士,南京大学硕士。美国威士康星、伊利诺伊和佛罗里达大学访问学者。被聘为西班牙Alcala大学、香港大学、新加坡国立大学和台湾大学客座教授。1991年当选中国科学院院士。游效曾教授先后任南京大学配位化学研究所所长,国家重点实验室和化学化工学院学术     

缅怀我们的导师——张滂院士

2011年11月29日,我们敬爱的导师张滂院士与世长辞。噩耗传来,作为学生的我们悲痛万分。师恩难忘,谨以此文作为对先生的纪念,并表达我们对先生的感谢与怀念之情。张滂先生早年就读于西南联大,毕业后曾作为老一辈有机化学家吴学周先生的助手开展研究工作。1945年留学英国,先后就读于利兹大学和剑桥大学,1949年7月获得有机化学博士学位。据了解,张滂先生是第一位获得剑桥大学博士学位的中国人。张先生于新中国成立之际回国效力,投身于祖国的教育和科技事业,先后任教于燕京大学和北京大学。     

《广州化学》征稿细则

<正>一、投稿要求1.稿件内容须符合本刊的报导宗旨,论点鲜明,数据可靠,文字简练。来稿文责自负。2.接受网上投稿。投稿信箱:gzhx@gic.ac.cn3.来稿一经刊出,酌付稿酬,并赠送当期杂志。     

离子色谱-直接电导法测定碱土金属和过渡金属离子

本文报道离子色谱-直接电导法测定碱土金属和过渡金属离子。研究了流动相pH值、乙二胺浓度及柠檬酸和酒石酸浓度对金属离子分离的影响。结果表明,以乙二胺-柠檬酸为流动相可以同时分离碱土金属和过渡金属离子。用乙二胺-酒石酸作为流动相可以分离碱土金属离子。方法检出限为0.09~1.88 mg/L,加标回收率为97.6%~98.7%。该方法用于叶面肥试样的分析,结果良好。     

《应用化学》2020年征订启事

《应用化学》创刊于1983年,是经国家科委批准向国内、国外公开发行的学术性期刊。由中国科学院主管,中国科学院长春应用化学研究所和中国化学会主办,科学出版社出版。为中国科技核心期刊。《应用化学》设有综合评述、研究论文、研究简报栏目。出版周期短,报道新成果快。《应用化学》期刊被14家国内外重要检索机构、文摘收录。《应用化学》面向科研单位、大专院校和化学化工领域的科研技术人员。本刊承揽各类化学、化工材料、分析测试仪器及各类化学产品介绍和相关领域科技信息等广告业务。     

《广州化学》征稿细则

[1]稿件内容须符合本刊的报道宗旨,论点鲜明,数据可靠,文字简练。[2]题目论文题目应准确、简明地表达文章的主题内容,字数不超过20字。不应有非规范的缩略词、符号、代号。文内标题序号用阿拉伯数字,以＂1、1.1、1.1.1＂三级标题表示。标题一般不超过15个字,不加标点符号。[3]署名作者署名一般不超过5人。首页脚注第...     

实验探究钢铁的腐蚀

在电化学的教学中,很多教师普遍认为钢铁在酸性环境下发生析氢腐蚀,在碱性或中性环境下发生吸氧腐蚀。。笔者对此进行了多次实验,发现此结论有误。这里和同行们一起探讨。     

探究教学论析

探究教学是现代西方料学教学理论和实践的重要基础之一。它以培养学生的探究素养和探究精神为主旨,强调科学方法、科学过程和科学观念的教育。突出学习中的学会探究和探究中学会学习。探究教学不仅有丰富的教育观,也有深厚的方法论。这就是探究教学的过程论。教学模式和教学策略。     

《应用化学》2013年征订启事

《应用化学》创刊于1983年,是经国家科委批准向国内、国外公开发行的学术性期刊。由中国科学院主管,中国化学会和中国科学院长春应用化学研究所主办,科学出版社出版。为中国科技核心期刊。《应用化学》设有综合评述、研究论文、研究简报、研究快报栏目。出版周期短,报道新成果快。《应用化学》期刊被14家国内外重要检索机构、文摘收录。     

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%.     

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.     

A general and convenient synthesis of 4-(tosylmethyl)semicarbazones and their use in amidoalkylation of hydrogen,heteroatom, and carbon nucleophiles

A general synthesis of previously unknown semicarbazone-based α-amidoalkylating reagents, 4-(tosylmethyl)semicarbazones, has been developed. The synthesis involved three-component condensation of semicarbazones of aliphatic or aromatic aldehydes with the same or other aldehydes and p-toluenesulfinic acid. The scope and limitations of this reaction were investigated. The compounds obtained were demonstrated to be an efficient α-(4-semicarbazono)alkylating agents. They were reacted with H- (sodium borohydride), O- (sodium methylate), S- (sodium phenylthiolate), N- (pyrrolidine, sodium succinimide), P- (trialkyl phosphites), and C-nucleophiles (sodium diethyl malonate) to give the corresponding products of the tosyl group substitution, 4-substituted semicarbazones, including analogues of nitrofurazone. Among the prepared compounds tested in vitro for antibacterial and antifungal activity, three nitrofuryl-containing semicarbazones exhibited high biological activities with minimum inhibitory concentration (MIC) values of 8–32 μg/mL.     

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.     

Synthesis of novel chiral bidentate hydroxyalkyl-N-heterocyclic carbene ligands and their application in palladium-catalyzed Mizoroki–Heck couplings and asymmetric addition of diethylzinc to benzaldehyde

A small library of new chiral bidentate hydroxyalkyl-imidazolium salts 1 is conveniently synthesized on multi-gram scale from inexpensive and commercially available chiral pool amino acids. The corresponding carbenes, generated by deprotonation of imidazolium salts 1, in combination with palladium(II) chloride were tested in the Mizoroki–Heck coupling reaction. The most significant results in terms of yields and reactivities were achieved with low catalyst loading. The catalytic activities of these imidazolium salts were also investigated in the asymmetric addition of diethylzinc to benzaldehyde. The use of MgO nanoparticles as an additive in conjunction with these ligands played a crucial role in increasing the efficiency of these reactions.     

α-Amino acid derived enaminones and their application in the synthesis of N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates and other heterocycles

A new and simple synthesis of novel N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates, which exist in equilibrium with their 4-oxo tautomers, has been developed in two steps starting from N-protected α-amino acids. The key intermediates are enaminones, which can also be isolated, characterized, and used for the construction of other functionalized heterocycles, before they spontaneously decompose to pyrrole products. 4-Hydroxypyrroles are prone to partial aerial oxidation but can be efficiently alkylated or reduced to stable polysubstituted pyrrolidine derivatives.     

Specific intramolecular aromatic CH insertion of diazosulfonamides

The chemoselectivity in the intramolecular CH insertion of various diazosulfonamides has been experimentally studied. The results reveal that the aliphatic 1,4-, 1,5-, or 1,6-C(sp³)?H insertions of diazosulfonamides are not accessible, while the aromatic 1,5-C(sp²)?H insertion can be realized specifically by adjusting the diazo-adjacent group. In addition, the general chemoselectivities in the intramolecular CH insertions of diazosulfonyl compounds are summarized. Generally, diazosulfones undergo both aromatic 1,5-C(sp²)?H and aliphatic 1,5- and 1,6-C(sp³)?H insertions, while diazosulfonates undergo aliphatic 1,5- and 1,6-C(sp³)?H insertions. However, diazosulfonamides only undergo aromatic 1,5-C(sp²)?H insertion.     

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.     

Microwave-assisted copper-catalyzed stereoselective ring expansion of three-membered heterocycles with α-diazo-β-dicarbonyl compounds

Microwave-assisted copper-catalyzed ring expansions of three-membered heterocycles with α-diazo-β-dicarbonyl compounds were investigated. Thiiranes generated 3-acyl-5,6-dihydro-1,4-oxathiines in the presence of copper sulfate and trans-3-acyl-5,6-dihydro-1,4-oxathiines as stereospecific products for 1,2-disubstituted cis-thiiranes through an intramolecular S_N2 process. Oxiranes gave rise to 2-acyl-5,6-dihydro-1,4-dioxines under the catalysis of copper hexafluoroacetylacetonate and cis-3-acyl-5,6-dihydro-1,4-dioxines as stereospecific products for 1,2-disubstituted cis-oxiranes via an intimate ion-pair mechanism. The current method provides a direct and simple strategy in efficient preparation of 3-acyl-5,6-dihydro-1,4-oxathiines and 2-acyl-5,6-dihydro-1,4-dioxines, important agents in medicinal and agricultural chemistry, from readily available thiiranes and oxiranes, respectively.     

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.