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2,2-diphenyloxathiirane | 60870-95-3

中文名称
——
中文别名
——
英文名称
2,2-diphenyloxathiirane
英文别名
3,3-Diphenyloxathiirane
2,2-diphenyloxathiirane化学式
CAS
60870-95-3
化学式
C13H10OS
mdl
——
分子量
214.288
InChiKey
VDSBZDLFZWNBKI-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    314.8±52.0 °C(Predicted)
  • 密度:
    1.256±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.4
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    37.8
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    参考文献:
    名称:
    低温氩基质中取代氧杂环丙烷的光化学形成和反应性
    摘要:
    衍生自脂肪族和脂环族硫酮的硫代羰基 S-氧化物(亚砜)在 10 K 的氩基质中进行辐照,并通过计算和实验红外光谱的比较来鉴定所得氧硫杂环丙烷。在 10 K 光解后,根据取代模式,氧杂环丙烷经历 H 位移反应或区域选择性环扩大以形成相应的硫酯。将基体材料加热到 38-40 K 后,氧杂环丙烷进行快速脱硫以产生相应的酮。B3LYP/6-311+G(3df,3pd) 水平的密度泛函理论 (DFT) 计算表明氧硫杂环丁烷的脱硫作为双分子过程发生,活化焓接近 0 kcal mol–1。
    DOI:
    10.1002/ejoc.201100695
  • 作为产物:
    描述:
    [苯基(亚磺酰基)甲基]苯 为溶剂, 反应 0.02h, 生成 2,2-diphenyloxathiirane
    参考文献:
    名称:
    低温氩基质中取代氧杂环丙烷的光化学形成和反应性
    摘要:
    衍生自脂肪族和脂环族硫酮的硫代羰基 S-氧化物(亚砜)在 10 K 的氩基质中进行辐照,并通过计算和实验红外光谱的比较来鉴定所得氧硫杂环丙烷。在 10 K 光解后,根据取代模式,氧杂环丙烷经历 H 位移反应或区域选择性环扩大以形成相应的硫酯。将基体材料加热到 38-40 K 后,氧杂环丙烷进行快速脱硫以产生相应的酮。B3LYP/6-311+G(3df,3pd) 水平的密度泛函理论 (DFT) 计算表明氧硫杂环丁烷的脱硫作为双分子过程发生,活化焓接近 0 kcal mol–1。
    DOI:
    10.1002/ejoc.201100695
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文献信息

  • Carbonyl sulfides as possible intermediates in the photolysis of oxathiiranes
    作者:Lars Carlsen、James P. Snyder、Arne Holm、Erik Pedersen
    DOI:10.1016/s0040-4020(01)92060-5
    日期:1981.1
    Diphenyl oxathiirane, formed by irradiation of thiobenzophenone S-oxide at 77 K, is photochemically converted into a blue, thermally unstable compound which decomposes at ca 100–110 K (λmax 550 nm, (ϵ ca 11,000). Lack of change in magnetic susceptibility during the light induced conversion of sulfine to ketone via the oxathiirane and the subsequent blue intermediate implies the absence of triplet and
    二苯氧杂环乙烷是由硫代二苯甲酮S-氧化物在77 K的辐射下形成的,被光化学转化为一种蓝色的热不稳定化合物,其在大约100–110 K时分解(λ最大550 nm,(ϵ大约11,000))。到酮经由oxathiirane和随后的蓝色中间锍化的光致转换期间敏感性意味着不存在三重态和双自由基单峰瞬变的。未知硫化羰的功能,R 2 COS,从而出现作为制造的有力候选可见吸收。
  • Preparation of a thermoformed polyarylene sulfide container
    申请人:KUREHA KAGAKU KOGYO KABUSHIKI KAISHA
    公开号:EP0288308A2
    公开(公告)日:1988-10-26
    A crystallized, thin-walled container, suitable for packaging foodstuffs which are subsequently heated, is obtained by thermoforming a sheet which has a crystallinity index of below 15% and an elongation of not less than 100% at room temperature and which has been obtained from a poly(arylene sulfide) which has as substantially linear structure, has not less than 70 wt% of a repeating unit and has a logarithmic viscosity number of 0.2 to 1.0 in a solution of l-chloronaphthalene (concentration of 0.4 g/dl at a temperature of 208°C).
    一种结晶的薄壁容器,适用于包装随后加热的食品,它是通过热成型获得的,这种片材的结晶度指数低于 15%,室温下的伸长率不小于 100%,它是由聚芳基硫醚获得的,这种聚芳基硫醚基本上是线性结构,重复单元的重量百分比不小于 70%。 在对氯萘溶液(浓度为 0.4 克/分升,温度为 208 摄氏度)中的对数粘度值为 0.2 至 1.0。
  • Polyarylene sulfide resin composition
    申请人:POLYPLASTICS CO. LTD.
    公开号:EP0327300A1
    公开(公告)日:1989-08-09
    A polyarylene sulfide composition is improved in impact resistance and comprises (A) 100 parts by weight of a polyarylene sulfide resin and (B) 0.5 to 50 parts by weight of a graft copolymer comprising (a) an olefin copolymer comprising an α-olefin and a glycidyl ester of an α,β-­unsaturated acid and (b) one or more polymers or copolymers constituted of a repeating unit represented by the following general formula (1), both of which are chemically bonded to each other to form a branched or crosslinked structure: wherein R stands for a hydrogen atom or a lower alkyl group and X is an alkyl having 1 to 8 carbon atoms, straight or branched, phenyl or cyano.
    一种聚芳硫醚组合物的抗冲击性得到改善,包括 (A) 100 重量份的聚芳硫醚树脂和 (B) 0.5 至 50 份(重量)接枝共聚物,包括(a)由α-烯烃和α,β-不饱和酸的缩水甘油酯组成的烯烃共聚物和(b)由下式(1)所代表的重复单元构成的一种或多种聚合物或共聚物,两者相互化学键合以形成支链或交联结构: 其中 R 代表氢原子或低级烷基,X 代表具有 1 至 8 个碳原子的直链或支链烷基、苯基或氰基。
  • Processes for the production of arylene thioether oligomers and copolymers
    申请人:KUREHA KAGAKU KOGYO KABUSHIKI KAISHA
    公开号:EP0508705A2
    公开(公告)日:1992-10-14
    Disclosed herein are a process for the preparation of a carboxylated arylene thioether oligomer, in which an alkali metal sulfide is caused to act on a poly(arylene thioether) so as to depolymerize the poly(arylene thioether), thereby preparing an alkali thiolate-containing oligomer, and a carboxylating agent is then caused to act on the alkali thiolate-containing oligomer, thereby forming the carboxylated arylene thioether oligomer, and a process for the production of an arylene thioether copolymer, wherein the carboxylated arylene thioether oligomer alone, which has been obtained in accordance with this preparation process, or a mixture of the carboxylated oligomer in an amount of at least 50 wt.% and another carboxylic compound in an amount less than 50 wt.% is reacted with an alkylenediol or an alkylenediol and a polyester or an alkylene diol and a lactone.
    本发明公开了一种制备羧基化芳基烯硫醚低聚物的工艺,其中使碱金属硫化物作用于聚(芳基烯硫醚),使聚(芳基烯硫醚)解聚,从而制备含碱硫酸盐的低聚物,然后使羧化剂作用于含碱硫酸盐的低聚物,从而形成羧基化芳基烯硫醚低聚物、其中,根据该制备工艺得到的羧基化芳基硫醚低聚物,或羧基化低聚物(至少 50 wt.与烷二醇或烷二醇和聚酯或亚烷基二元醇和内酯反应。
  • Production process of alkylene thioether-arylene thioether copolymer
    申请人:KUREHA KAGAKU KOGYO KABUSHIKI KAISHA
    公开号:EP0524827A1
    公开(公告)日:1993-01-27
    Disclosed herein is a process for the production of an alkylene thioether-arylene thioether copolymer, which comprises copolymerizably reacting a compound having at least one alkali thiolate group and obtained by causing an alkali metal sulfide to act on a poly(arylene thioether) in a water-containing polar organic solvent so as to depolymerize the poly(arylene thioether) with a dihalogen-substituted aliphatic compound in a water-containing polar organic solvent.
    本文公开了一种亚烷基硫醚-芳基硫醚共聚物的生产工艺,该工艺包括在含水的极性有机溶剂中,使具有至少一个碱硫酸盐基团并通过使碱金属硫化物作用于聚芳基硫醚而获得的化合物与二卤代脂肪族化合物发生共聚反应,从而使聚芳基硫醚解聚。
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