Artem M. Mishchenko , Yulian L. Lishchenko , Andriy V. Kozytskiy , Kateryna M. Konysheva , Yulia A. Satska , Serhiy V. Ryabukhin , Dmytro M. Volochnyuk , Sergey V. Kolotilov , Yuliya V. Rassukana
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It was found that pyrolysis of Et<sub>4</sub>NBH<sub>4</sub> in suspension in silicone fluid led to the mixtures of (Et<sub>4</sub>N)<sub>2</sub>[B<sub>10</sub>H<sub>10</sub>] and (Et<sub>4</sub>N)<sub>2</sub>[B<sub>12</sub>H<sub>12</sub>]. Pyrolysis of Et<sub>4</sub>NBH<sub>4</sub> in <em>n</em>-decane or decalin resulted in Et<sub>4</sub>N[B<sub>3</sub>H<sub>8</sub>] as a primary product. An increase of reaction time in <em>n</em>-decane or both time and temperature in decalin yielded the mixture of (Et<sub>4</sub>N)<sub>2</sub>[B<sub>10</sub>H<sub>10</sub>], (Et<sub>4</sub>N)<sub>2</sub>[B<sub>12</sub>H<sub>12</sub>] and other compounds. It was shown that the degree of conversion of Et<sub>4</sub>NBH<sub>4</sub> into Et<sub>4</sub>N[B<sub>3</sub>H<sub>8</sub>] on time in <em>n</em>-decane at 174 °C and decalin at 180 °C linearly depends on time. Several methods for purification of <em>closo</em>-decaborate from other pyrolysis products were checked. A synthetic procedure for preparation of <em>closo</em>-decaborate from 60 g of Et<sub>4</sub>NBH<sub>4</sub> was proposed, yielding 2.85 g of (Bu<sub>3</sub>NH)<sub>2</sub>[B<sub>10</sub>H<sub>10</sub>] (95 % purity) in one run.</div></div>","PeriodicalId":20278,"journal":{"name":"Polyhedron","volume":"279 ","pages":"Article 117646"},"PeriodicalIF":2.4000,"publicationDate":"2025-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Preparation of closo-decaborate by pyrolysis of tetraethylammonium borohydride: Revision and optimization for large-scale production\",\"authors\":\"Artem M. Mishchenko , Yulian L. Lishchenko , Andriy V. Kozytskiy , Kateryna M. Konysheva , Yulia A. Satska , Serhiy V. Ryabukhin , Dmytro M. Volochnyuk , Sergey V. Kolotilov , Yuliya V. 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引用次数: 0
摘要
研究了四乙基硼氢化铵热解合成碳硼烷的关键化合物——近癸酸盐([B10H10]2 - as聚烷基铵盐)的几种制备方法。所研究的反应包括分解温度、液体介质、压力和反应时间的变化。产物通过11B和1H NMR谱分析,在某些情况下,通过ir谱分析。研究发现,悬浮态Et4NBH4在有机硅液中热解生成(Et4N)2[B10H10]和(Et4N)2[B12H12]的混合物。Et4NBH4在正癸烷或十氢化萘中热解生成主要产物Et4N[B3H8]。在正十烷中增加反应时间或在十烷中增加反应时间和温度,可以得到(Et4N)2[B10H10]、(Et4N)2[B12H12]等化合物的混合物。结果表明,在174℃的正癸烷和180℃的十萘中,Et4NBH4及时转化为Et4N[B3H8]的程度与时间呈线性关系。考察了几种从其他热解产物中提纯近癸酸盐的方法。提出了一种以60 g Et4NBH4为原料,一次可制得(bu3nh2 [B10H10]) 2.85 g(纯度95%)的合成方法。
Preparation of closo-decaborate by pyrolysis of tetraethylammonium borohydride: Revision and optimization for large-scale production
Several methods for the preparation of closo-decaborate ([B10H10]2− as polyalkylammonium salts) – a key compound for the synthesis of carborane – by pyrolysis of tetraethylammonium borohydride were examined. The studied reactions included variations in decomposition temperature, liquid medium, pressure and reaction time. The products were analyzed by 11B and 1H NMR spectroscopy, and, in some cases, by IR-spectroscopy. It was found that pyrolysis of Et4NBH4 in suspension in silicone fluid led to the mixtures of (Et4N)2[B10H10] and (Et4N)2[B12H12]. Pyrolysis of Et4NBH4 in n-decane or decalin resulted in Et4N[B3H8] as a primary product. An increase of reaction time in n-decane or both time and temperature in decalin yielded the mixture of (Et4N)2[B10H10], (Et4N)2[B12H12] and other compounds. It was shown that the degree of conversion of Et4NBH4 into Et4N[B3H8] on time in n-decane at 174 °C and decalin at 180 °C linearly depends on time. Several methods for purification of closo-decaborate from other pyrolysis products were checked. A synthetic procedure for preparation of closo-decaborate from 60 g of Et4NBH4 was proposed, yielding 2.85 g of (Bu3NH)2[B10H10] (95 % purity) in one run.
期刊介绍:
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