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化驗
98%
形狀
liquid
折射率
n20/D 1.446 (lit.)
bp
135-136 °C (lit.)
密度
0.8 g/mL at 25 °C (lit.)
儲存溫度
2-8°C
SMILES 字串
C#CCCCCC#C
InChI
1S/C8H10/c1-3-5-7-8-6-4-2/h1-2H,5-8H2
InChI 密鑰
DSOJWVLXZNRKCS-UHFFFAOYSA-N
一般說明
1,7-Octadiyne is a terminal bis-alkyne and participates in the formation of uranium(IV) vinyl complexes. It reacts with frustrated Lewis pair P(o-tolyl)3/B(C6F5)3 by acetylene C-C coupling to yield the zwitterionic product. It undergoes the reductive cyclization during reaction with Re2Cl4(μ-dppm)2 (dppm = Ph2PCH2PPh2) and affords quadruply bonded dirhenium(III) complex Re2Cl3(μ,η2-C8H7)(μ-dppm)2.
訊號詞
Warning
危險分類
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
73.4 °F - closed cup
閃點（°C）
23 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
Chao Chen et al.
Chemical communications (Cambridge, England), 46(20), 3580-3582 (2010-04-09)
The frustrated Lewis pair P(o-tolyl)(3)/B(C(6)F(5))(3) reacts with 1,7-octadiyne by acetylene C-C coupling to yield the zwitterionic product 2a. In contrast, the P(o-tolyl)(3)/B(C(6)F(5))(3) Lewis pair reacts with 1,6-heptadiyne by a sequence involving 1,1-carboboration of a terminal acetylene to eventually yield the
Boris Kosog et al.
Journal of the American Chemical Society, 134(30), 12792-12797 (2012-06-29)
The previously reported uranium(III) complex [(((Ad)ArO)(3)N)U(III)(DME)] (1; Ad = adamantane, DME = 1,2-dimethoxyethane) reacts with the terminal bis-alkynes 1,7-octadiyne or 1,6-heptadiyne in C-C-coupling reactions to form the uranium(IV) vinyl complexes [{(((Ad)ArO)(3)N)U(IV)}(2)(μ-η(2):η(1)-1,2-(CH)(2)-cyclohexane)] (2) and [{(((Ad)ArO)(3)N)U(IV)}(2)(μ-η(2):η(2)-1,2-(CH)(2)-cyclopentane)] (3). With the monoalkynes 1-hexyne or
A Novel Example of the Reductive Cyclization of a Diyne at a Re-Re Triple Bond: The Reaction of Re2Cl4 (?-dppm) 2 with 1, 7-Octadiyne.
Ganesan M, et al.
Organometallics, 22(4), 870-872 (2003)
Christina A Braun et al.
Dalton transactions (Cambridge, England : 2003), 48(27), 10210-10219 (2019-06-14)
A new di(isopropoxy)boryl -B(OiPr)2 tellurophene precursor is described, from which several previously inaccessible phosphorescent borylated tellurophenes are formed via exchange of the -OiPr groups. One such tellurophene Mes(iPrO)B-Te-6-B(OiPr)Mes, bearing a sterically encumbered mesityl (Mes) substituent at each boron center, exhibits
Shasha Wang et al.
Scientific reports, 7(1), 12712-12712 (2017-10-07)
We developed an efficient one-pot metal-free click polymerization procedure for the synthesis of 3,5-disubstituted polypyrazoles with high yields, high molecular weights, and narrow molecular weight distribution. The method involved two click reactions in a one-pot synthesis. The first reaction was
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