Synthetic methods for, and structural and spectroscopic characteristics of sulfur-containing macroheterocycles are discussed. The synthesis of oligothiamacrocycloalkanes is based on the reaction of α, ò-dihaloalkanes with alkali α,ò-alkanedithiolates to form 12-42-membered macroheterocycles with 2-6 sulfur atoms in the ring. Oxathiamacrocycloalkanes containing sulfur and oxygen atoms in the ring have been prepared by reaction of aromatic 1,2-dithiols or 2-mercaptophenols with aliphatic α-ò-dihalo derivatives. The synthesis of thiamacrocycloalkanes involves the reaction of dimethyl ethers or α,ò-alkanedicarboxylic acid dichlorides with α,ò-alkanediamines followed by reduction of the macroheterocyclic diamides with LiAlH4 or B2H6. Oxathiaazamacrocycloalkanes have been prepared in a similar way by reaction of dicarboxylic acid dichlorides with α,ò-oxaalkanediamines as well as by reaction of chlorosulfonyl-β-lactams with glycols.A general synthetic route to oligothiacyclophanes is the reaction of bis-(bromomethyl) substituted arenes with bis-(mercaptomethyl)benzenes. Analogously, sulfur-containing cyclopyridinophanes have been prepared by reaction of 2,6-bis(bromomethyl)pyridine with α,ò-alkanedithiols. For the synthesis of macrocyclic compounds containing one, two, or several thiophene rings, some procedures based on intra-and intermolecular acylation of ò-thienylalkanecarboxylic acid chlorides, acyloin condensation of 2,5-bis(carbalkoxyalkyl)thiophenes, and intramolecular alkylation of ò-haloalkyl substituted β-keto esters of the thiophene series have been developed.Synthetic routes to macroheterocycles containing di-and polysulfide groups are discussed. The synthesis involves sulfurization of mesitylene or 1,3-dimethoxybenzene with disulfur dichloride or sulfur dichloride as well as the oxidation of dithiols.The synthesis of bi-and trimacrocyclic compounds is based on the reaction of 1,3,5-tris(mercaptoalkyl)benzenes with tris(bromoalkyl)-methanes or l,3,5-tris[4-(mercaptomethyl)phenyl]-benzene with 1,3,5-tris-[4-(bromomethyl)phenyl] benzene.Some methods for the synthesis of sulfur-containing macroheterocycles containing silicon, tellurium, or iron are considered.The structures of the sulfur-containing macroheterocycles are discussed using the results of X-ray diffraction, H NMR, IR, and UV spectroscopy as well as their electroconductive and magnetic properties.
讨论了含硫大杂环化合物的合成方法、结构和光谱特征。以α,_-二卤代烷与碱α,_-烷二硫醇反应,合成了含2-6个硫原子的12-42元大杂环。通过芳香族1,2-二硫醇或2-巯基酚与脂肪族α-二卤代衍生物的反应,制备了含硫和氧原子的氧杂硫大环烷烃。硫大环烷烃的合成包括二甲醚或α,_烷二羧酸二氯化物与α,_烷二胺的反应,然后用LiAlh4或B2H6还原大杂环二胺。以二羧酸二氯化物与α,_-恶烷二胺反应,以及氯磺酰-β-内酰胺与乙二醇反应制备了氧杂氮杂大环烷,双(溴甲基)取代芳烃与双(巯基甲基)苯的反应是合成低聚噻环烷的一般途径。以2,6-双(溴甲基)吡啶与α,_-烷烃二硫醇反应制备了含硫环吡啶衍生物。对于含有一个、两个或多个噻吩环的大环化合物的合成,基于-噻吩烷羧酸氯化物的分子内和分子间酰化、2,5-双(碳烷氧基烷基)噻吩的酰偶姻缩合和-卤代烷基取代的噻吩β-酮酯的分子内烷基化的一些步骤。研究了含二硫化物和多硫化物的大杂环化合物的合成路线。合成过程中,均三甲苯或1,3-二甲氧基苯与二硫二氯化物或二硫二氯化物硫化,并氧化二硫醇,以1,3,5-三(巯基烷基)苯与三(溴代烷基)-甲烷或L,3,5-三[4-(巯基甲基)苯基]-苯的反应为基础,合成了双和三丙烯基环化合物。以1,3,5-三-[4-(溴甲基)苯基]苯为原料,研究了含硅、碲或铁的含硫大杂环化合物的合成方法,并用X射线衍射、核磁共振、红外光谱、紫外光谱等分析结果,讨论了含硫大杂环化合物的结构及其导电性和磁性。
期刊ISSN
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1998-9539 |
最新的影响因子
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1.4 |
最新CiteScore值
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1.13 |
最新自引率
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30.10% |
期刊官方网址
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期刊投稿网址
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通讯地址
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偏重的研究方向(学科)
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CHEMISTRY, MULTIDISCIPLINARY- |
出版周期
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平均审稿速度
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出版年份
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0 |
出版国家/地区
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RUSSIA |
是否OA
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No |
SCI期刊coverage
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Science Citation Index Expanded(科学引文索引扩展) |
NCBI查询
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PubMed Central (PMC)链接 全文检索(pubmed central) |
最新中科院JCR分区
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大类(学科)
小类(学科)
JCR学科排名
化学
CHEMISTRY, MULTIDISCIPLINARY(化学,跨学科) 3区
126/171
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最新的影响因子
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1.4 | |||||||
最新公布的期刊年发文量 |
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总被引频次 | 482 | |||||||
特征因子 | 0.000600 | |||||||
影响因子趋势图 |
2007年以来影响因子趋势图(整体平稳趋势)
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最新CiteScore值
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1.13
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引文计数(2018)
文献(2015-2017)
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197次引用
174篇文献
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文献总数(2014-2016) | 174 | ||||||||||
被引用比率
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56% | ||||||||||
SJR
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0.313 | ||||||||||
SNIP
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0.66 | ||||||||||
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scopus涵盖范围 |
scopus趋势图
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本刊同领域相关期刊
|
|
期刊名称 | IF值 |
Avian Biology Research | 0.6 |
CHIMIA | 1.2 |
Chemija | 0.6 |
AFINIDAD | 0.3 |
QUIMICA NOVA | 0.8 |
RSC Advances | 3.9 |
ChemPlusChem | 3.4 |
ChemistryOpen | 2.3 |
CHEMICKE LISTY | 0.6 |
本刊同分区等级的相关期刊
|
|
期刊名称 | IF值 |
Avian Biology Research | 0.6 |
CHIMIA | 1.2 |
Open Chemistry | 2.3 |
ChemistrySelect | 2.1 |
CHEMISTRY LETTERS | 1.6 |
Macroheterocycles | 1.4 |
HETEROATOM CHEMISTRY | 0.3 |
Journal of Chemistry | 3 |
COMPTES RENDUS CHIMIE | 1.6 |
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