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1,1,3,3-四(二甲基氨基)-1,3-二磷杂环丁二烯 | 103678-18-8

中文名称
1,1,3,3-四(二甲基氨基)-1,3-二磷杂环丁二烯
中文别名
——
英文名称
1,1,3,3-tetrakis(dimethylamino)-1λ5,3λ5-diphosphete
英文别名
1,1,3,3-Tetrakis(dimethylamino)-diphosphet;1,1,3,3-Tetrakis(dimethylamino)-1λ5,3λ5-diphosphet;1,3-Diphosphacyclobutadiene, 1,1,3,3-tetra(dimethylamino)-;1-N,1-N,1-N',1-N',3-N,3-N,3-N',3-N'-octamethyl-1λ5,3λ5-diphosphacyclobuta-1,3-diene-1,1,3,3-tetramine
1,1,3,3-四(二甲基氨基)-1,3-二磷杂环丁二烯化学式
CAS
103678-18-8
化学式
C10H26N4P2
mdl
——
分子量
264.291
InChiKey
HMKOERUGKYBVQK-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:
    328.3±25.0 °C(Predicted)
  • 密度:
    1.07±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.9
  • 重原子数:
    16
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    13
  • 氢给体数:
    0
  • 氢受体数:
    4

SDS

SDS:4b867e69458d1f8dd1356764fc0fcdaa
查看

反应信息

  • 作为反应物:
    描述:
    1,1,3,3-四(二甲基氨基)-1,3-二磷杂环丁二烯叔丁醇 作用下, 以 乙醚 为溶剂, 反应 0.17h, 生成 Bis(dimethylamino)phosphorylmethyliden-methyl-bis(dimethylamino)phosphoran
    参考文献:
    名称:
    Fluck, Ekkehard; Lange, Karsten; Heckmann, Gernot, Phosphorus, Sulfur and Silicon and the Related Elements, 1992, vol. 72, # 1-4, p. 49 - 54
    摘要:
    DOI:
  • 作为产物:
    描述:
    methyl-bis(dimethylamino)difluorophosphorane正丁基锂 作用下, 以 正己烷正戊烷 为溶剂, 反应 2.0h, 以33.9%的产率得到1,1,3,3-四(二甲基氨基)-1,3-二磷杂环丁二烯
    参考文献:
    名称:
    Svara, Juergen; Fluck, Ekkehard; Riffel, Heinz, Zeitschrift fur Naturforschung, Teil B: Anorganische Chemie, Organische Chemie, 1985, vol. 40, # 10, p. 1258 - 1263
    摘要:
    DOI:
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文献信息

  • 6-Pyridyl-1-aza-2λ<sup>5</sup>,4λ<sup>5</sup>-diphosphinin - ein 2,2′-Bipyridin-Analogon/ 6-Pyridyl-1-aza-2λ<sup>5</sup>,4λ<sup>5</sup>-diphosphinine - a 2,2′-Bipyridine Analogue
    作者:Gernot Heckmann、Stefan Plank、Ekkehard Fluck、Anahita Dashti-Mommertz、Bernhard Neumüller
    DOI:10.1515/znb-1999-1123
    日期:1999.11.1

    1,1,3,3-Tetrakis(dimethylamino)-1λ5,3λ5-diphosphete, (1), reacts with 2-cyano-pyridine to yield 6- pyridyl-1-aza-2λ5,4A5-diphosphinine (3). 3 is characterized by its 1H , 31P, and 13C NMR, mass, and IR spectra as well as the results of the X-ray structure analysis.

    1,1,3,3-四(二甲氨基)-1λ5,3λ5-二膦酯(1)与2-氰基吡啶反应,生成6-吡啶基-1-氮杂-2λ5,4A5-二膦环(3)。通过其1H,31P和13C NMR,质谱和红外光谱以及X射线结构分析结果表征3。
  • Ein weiteres 2λ<sup>5</sup>,4λ<sup>5</sup>-Diphosphapyridin: 2,2,4,4-Tetrakis-(dimethylamino)-6- amino-1-aza-2λ<sup>5</sup>,4λ<sup>5</sup>-diphosphinin / A Further 2λ<sup>5</sup>,4λ<sup>5</sup>-Diphosphapyridine: 2,2,4,4-Tetrakis-(Dimethylamino)-6-amino-1-aza- 2λ<sup>5</sup>,4λ<sup>5</sup>-diphosphinine
    作者:Gemot Heckmann、Ekaterina Jonas、Ekkehard Fluck、Bernhard Neumüller
    DOI:10.1515/znb-1998-0410
    日期:1998.4.1

    2,2,4,4-Tetrakis-(dimethylamino)-6-amino-1-aza-2λ5,4λ5-diphosphinine (3) has been prepared by reacting 1,1,3,3-tetrakis(dimethylamino)-1λ5-3λ5-diphosphete (1) with bis(trimethylsilyl) carbodiimide (2) in a 2 : 1 molar ratio. Properties, 1H, 31P, and 13C NMR, mass, and IR spectra are reported and discussed. Compound 3 is further characterized by X-ray structure analysis.

    2,2,4,4-四(二甲基胺基)-6-基-1-氮杂-2λ5,4λ5-二膦杂环(3),是通过1,1,3,3-四(二甲基胺基)-1λ5-3λ5-二膦杂环(1)和双(三甲基基)腈基甲烷(2)在2:1的摩尔比下反应制备而成。报道和讨论了其性质,1H、31P和13C NMR,质谱和红外光谱。化合物3还通过X射线结构分析进行了进一步的表征。
  • Ein neuer Heterocyclus, 2λ<sup>3</sup>,4λ<sup>5</sup>-[1,2,4]-Oxadiphosphinin (2), als Ligand eines zweikernigen Eisenkomplexes / A New Heterocycle, 2λ<sup>3</sup>, 4λ<sup>5</sup> -[1,2,4]-Oxadiphosphinine (2), as Ligand of a Binuclear Iron Complex
    作者:Fred Rosche、Gernot Heckmann、Frank Weller、Ekkehard Fluck
    DOI:10.1515/znb-1996-1209
    日期:1996.12.1

    Preparation and properties of a coordination compound are described, in which a carbonyl group in bis[(dicarbonyl)(μ5-cyclopentadienyl)iron] is substituted by hitherto unknown octa- N-methyl-2λ3,4λ5-[1,2,4]-oxadiphosphinine-2,4,4,6-tetramine (2). The 1H , 31P, and 13C NMR spectra are recorded and discussed in detail. The molecular structure of the iron complex 4 is described and interpreted.

    描述了一种配位化合物的制备和性质,其中双[(二羰基)(μ5-环戊二烯基)]中的一个羰基被迄今为止未知的八- N-甲基-2λ3,4λ5-[1,2,4]-氧二环-2,4,4,6-四胺(2)所取代。记录并详细讨论了该化合物的 1H、31P 和 13C NMR 谱。描述并解释了配合物4的分子结构。
  • Fluck, Ekkehard; Neumueller, Bernhard; Heckmann, Gernot, Phosphorus and Sulfur and the Related Elements, 1988, vol. 37, p. 159 - 170
    作者:Fluck, Ekkehard、Neumueller, Bernhard、Heckmann, Gernot、Riffel, Heinz
    DOI:——
    日期:——
  • Ein (Phosphonioalkinyl)- und ein Acetyl(tetracarbonyl)eisen
    作者:Fred Rosche、Gernot Heckmann、Ekkehard Fluck、Frank Weller
    DOI:10.1002/zaac.19966220609
    日期:1996.6
    AbstractAus dem Reaktionsgemisch von 1,1,3,3‐Tetrakis(dimethylamino)‐1λ5,3λ5‐diphosphet, 1, und Fe(CO)5 können [Bis(dimethylamino)phosphoryl‐methyl]‐bis(dimethylamino)phosphonioethinyl}(tetracarbonyl)eisen, 4, und1,1,3,3‐Tetrakis(dimethylamino)‐1,4‐dihydro‐1λ5,3λ5‐[1,3]diphosphetium‐2‐carbonyl}(tetracarbonyl)eisen, 5, als kristalline Produkte isoliert werden. Die NMR‐, Massen‐ und IR‐Spektren der beiden Verbindungen werden mitgeteilt. Von 4 konnten die Kristall‐und Molekülstruktur ermittelt werden. Die Bindungsverhältnisse in 4 und 5 werden eingehend diskutiert.
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同类化合物

磷杂环戊-3-烯 9-磷杂二环[3.3.1]壬烷 4,8-二甲基-2-磷酸双环[3.3.1]壬烷 3,3-二甲基-1,2-二叔-丁基-二磷杂环丙烷 2-氧杂环烷酮,均聚物,氧代二-2,1-乙二基酯 1,3,4-三甲基-delta(3)-磷杂环戊烯-1,1-二氯化物 1,1,3,3-四(二甲基氨基)-1,3-二磷杂环丁二烯 1-Chlor-3,4-dimethyl-2(3)-phospholen {NiBr2-1.2-Bis-dimethylphosphino-aethan}Br cyclohex-1-enylphosphonic difluoride trans-2-Ethyl-phosphiran β-[PNtBu]4 (Z)-Cyclooctene; compound with bromine bis{1,2-bis(dimethylphosphino)ethane}di-iodoiron 2,4-di-tert.-butyl-1,1-dimethyl-1-stanna-2,5-cyclohexadiene [Pt(hydride)(1,2-bis(diethylphosphino)ethane)2](hexafluorophosphate) 2,3,4,5,6,7-hexamethyl-9,10,11,12-tetrakis(trifluoromethyl)-1,8-diphosphatetracyclo<6.2.2.02,7.03,6>dodeca-4,9,11-triene bis(triethylphosphine)-2,4,4-trimethylplatinacyclopentane Zr[TeSi(SiMe3)3]2(Te)(1,2-bis(dimethylphosphino)ethane)2 2,3-bis-trifluoromethyl-1-phospha-bicyclo[2.2.2]octa-2,5,7-triene 5-methoxy-2,2,3,3,7-pentamethyl-1,4,6-trioxa-5λ5-phospha-spiro[4.4]non-7-ene 3,4-Bis(2,2,3,3,4,4,5,5-decafluorpentyl)-1,2-dithiet 1,2,3,4,5-Pentamethyl-phosphole 1-oxide [n-BuB(CH2P-i-Pr2)3Ag(triethylphosphine)] 1-tert-butyl-3-phospholene brominanium 2,6,10,14-Tetramethyl-1,3,9,11-tetraoxa-2,6,10,14-tetraphospha-cyclohexadecane 2,6,10,14-tetrasulfide bis(triethylphosphine)-3,3-dimethylplatinacyclobutane 1,4,9,12-tetramethyl-1,4,9,12-tetraphosphacyclohexadeca-6,4-diene 1,4,9,12-tetraoxyde 1-methyl-octahydro-1-phospha-2,3-cyclo-dicyclopropa[a,cd]pentalene 1-oxide cis-2,6-dimethyl-1,3-dioxa-2,6-diphosphacyclo-octane 2,6-disulphide N-butyl-N-(3,4-dimethyl-1-oxo-2,5-dihydro-1lambda5-phosphol-1-yl)-3,4-dimethyl-1-oxo-2,5-dihydro-1lambda5-phosphol-1-amine oxolane;triiodovanadium trans-2,6-dimethyl-1,3-dioxa-2,6-diphosphacyclo-octane 2,6-disulphide 2,6-Dimethyl-[1,2,6]oxadiphosphinane 2,6-dioxide 1-cyclohexyl-phospholane 1-sulfide 1,4-Dicyclohexyl-2,2,3,3,5,5,6,6-octamethyl-[1,4,2,3,5,6]diazatetrasilinane 1-Chloro-2-methyl-phosphole 1-oxide 1-Isopropenyltellanyl-butane 2-Dimethylphosphanylethyl(dimethyl)phosphane;tetraiodohafnium 2,7-Dimethyl-[1,2,7]oxadiphosphepane 2,7-dioxide 9-methyl-(1rP,2cH,5cH,6cP)-9-phospha-tricyclo[4.2.1.02,5]nonane 9ξ-oxide bismethano-nickelacyclotridecahexaene ethylthiolato(methyl)(1,2-bis(diisopropylphosphino)ethane)platinum(II) 1-Chloro-2-methyl-phosphole 1-sulfide