摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

4H,8H-Benzo<1,2-c:4,5-c'>bis<1,2,5>selenadiazol-4,8-dion | 83274-16-2

中文名称
——
中文别名
——
英文名称
4H,8H-Benzo<1,2-c:4,5-c'>bis<1,2,5>selenadiazol-4,8-dion
英文别名
4H,8H-Benzo[1,2-c:4,5-c']bis[1,2,5]selenadiazol-4,8-dion;[1,2,5]selenadiazolo[3,4-f][2,1,3]benzoselenadiazole-4,8-dione
4H,8H-Benzo<1,2-c:4,5-c'>bis<1,2,5>selenadiazol-4,8-dion化学式
CAS
83274-16-2
化学式
C6N4O2Se2
mdl
——
分子量
318.012
InChiKey
PEANJGLRGPBZGN-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

  • 熔点:
    >300 °C
  • 沸点:
    541.7±60.0 °C(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -1.84
  • 重原子数:
    14.0
  • 可旋转键数:
    0.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    85.7
  • 氢给体数:
    0.0
  • 氢受体数:
    6.0

反应信息

点击查看最新优质反应信息

文献信息

  • Preparation and Crystal Structures of Tetracyanoquinodimethans Fused with [1,2,5]Selenadiazole Units
    作者:Takanori Suzuki、Chizuko Kabuto、Yoshiro Yamashita、Gunzi Saito、Toshio Mukai、Tsutomu Miyashi
    DOI:10.1246/cl.1987.2285
    日期:1987.11.5
    The title electron acceptors, TSDA (2) and BSDA (3), were prepared which crystallize isomorphously with the sulfur analogue, BTDA (1). The molecular interactions are enhanced in 2 and 3 compared with 1, which connect the molecules to form two-dimensionally expanded “sheet-like” networks and their infinite layers.
    制备出的标题电子受体 TSDA (2) 和 BSDA (3)与类似物 BTDA (1) 结晶同构。与 1 相比,2 和 3 中的分子相互作用得到了加强,它们将分子连接起来,形成了二维扩展的 "片状 "网络及其无限层。
  • Clathrate formation and molecular recognition by novel chalcogen-cyano interactions in tetracyanoquinodimethanes fused with thiadiazole and selenadiazole rings
    作者:Takanori Suzuki、Hiroshi Fujii、Yoshiro Yamashita、Chizuko Kabuto、Shoji Tanaka、Masako Harasawa、Toshio Mukai、Tsutomu Miyashi
    DOI:10.1021/ja00034a041
    日期:1992.4
    The intermolecular contacts between chalcogen atoms and cyano lone pairs were found to stabilize the crystalline state by electrostatic interaction. This interaction is one of the sources of the directionality in crystal packing of organic molecules and causes the formation of various types of inclusion lattices in the charge-transfer (CT) crystals of 1-3. By using highly selective formation of CT crystals with substituted aromatic hydrocarbons, particular isomers such as p-xylene or 2,6-dimethylnaphthalene (2,6-DMN) could be separated from the corresponding isomer mixtures. Lattice-related interaction plays a more significant role than molecular orbital interaction in the observed selectivity for para-disubstituted benzenes. However, the latter interaction is important for the recognition of 2,6-DMN from the 2,7 isomer.
  • Yamashita, Yoshiro; Tanaka, Shoji; Tomura, Masaaki, Phosphorus, Sulfur and Silicon and the Related Elements, 1992, vol. 67, # 1-4, p. 327 - 332
    作者:Yamashita, Yoshiro、Tanaka, Shoji、Tomura, Masaaki
    DOI:——
    日期:——
  • MUKAI, TOSIO;YAMASITA, JOSIO;SUDZUKI, TAKANORI
    作者:MUKAI, TOSIO、YAMASITA, JOSIO、SUDZUKI, TAKANORI
    DOI:——
    日期:——
  • NEIDLEIN, R.;TRAN-VIET, DAO;GIEREN, A.;KOKKINIDIS, M.;WILCKENS, R.;GESERI+, CHEM. BER., 1982, 115, N 8, 2898-2904
    作者:NEIDLEIN, R.、TRAN-VIET, DAO、GIEREN, A.、KOKKINIDIS, M.、WILCKENS, R.、GESERI+
    DOI:——
    日期:——
查看更多