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一般描述
1,7-辛二烯可作为乙烯的交联剂和来源，用于不同的Mori条件下的CEYM相关反应。
应用
用1，7-辛二烯研究了一系列简单的二前缀开环复分解的结构和反应速率。它也被用作研究等离子体聚合制备的微图案化表面。
警示用语：
Danger
危险声明
危险分类
Aquatic Chronic 3 - Asp. Tox. 1 - Flam. Liq. 2
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
50.0 °F - closed cup
闪点(°C)
10 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
M Ramiasa-MacGregor et al.
Nanoscale, 8(8), 4635-4642 (2016-02-09)
The wetting of a material can be tuned by changing the roughness on its surface. Recent advances in the field of nanotechnology open exciting opportunities to control macroscopic wetting behaviour. Yet, the benchmark theories used to describe the wettability of
B F P McVey et al.
Langmuir : the ACS journal of surfaces and colloids, 33(35), 8790-8798 (2017-05-30)
The role surface capping molecules play in dictating the optical properties of semiconductor nanocrystals (NCs) is becoming increasingly evident. In this paper the role of surface capping molecule polarity on the optical properties of germanium NCs (Ge NCs) is explored.
Rahul M Visalakshan et al.
ACS applied materials & interfaces, 11(31), 27615-27623 (2019-07-17)
The nature of the protein corona forming on biomaterial surfaces can affect the performance of implanted devices. This study investigated the role of surface chemistry and wettability on human serum-derived protein corona formation on biomaterial surfaces and the subsequent effects
Christopher Jay T Robidillo et al.
Nanoscale, 10(39), 18706-18719 (2018-10-03)
This study reports the preparation of functional bioinorganic hybrids, through application of the thiol-ene reaction, that exhibit catalytic activity and photoluminescent properties from enzymes and freestanding silicon nanocrystals. Thermal hydrosilylation of 1,7-octadiene and alkene-terminated poly(ethylene oxide)methyl ether with hydride-terminated silicon
Ian W Ashworth et al.
Chemical communications (Cambridge, England), 46(38), 7145-7147 (2010-09-08)
In the RCM reactions of a series of simple α,ω-dienes, the relative order of reactivity has been unambiguously determined showing that cyclohexene forms faster than cyclopentene or cycloheptene. 1,5-Hexadiene inhibits the RCM of 1,7-octadiene; 1,5-hexadiene cannot progress to the RCM
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