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일반 설명
Diphenylsilane is an organosilicon compound used as an amide bond coupling reagent & alkene hydrosilylation precursor.
애플리케이션
- Preparation of Bis diphenylsilane and Investigation of Its Cationic UV-Curing Material Properties: This study explores the synthesis and photosensitivity of a new material using diphenylsilane, emphasizing its potential in UV-curing applications (Y Liu et al., 2021, MDPI).
- Inkjet printing of blue phosphorescent light-emitting layer based on bis (3, 5-di (9 H-carbazol-9-yl)) diphenylsilane: Research on the use of diphenylsilane derivatives for developing blue phosphorescent materials for inkjet printing, which could be used in electronic displays (R Bail et al., 2018, RSC Advances).
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point (°F)
208.4 °F - closed cup
Flash Point (°C)
98 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
Diphenylsilane as a coupling reagent for amide bond formation
Sayes, Morgane, et al.
Green Chemistry, 19, 5060-5064 (2017)
Slawomir Rubinsztajn et al.
Macromolecular rapid communications, 42(5), e2000601-e2000601 (2020-12-04)
The reaction of poly(hydromethylsiloxane-co-methylphenylsiloxane) with zirconium (IV) n-propoxide in dry toluene leads to extensive scission of the siloxane chain and conversion of Si-H groups. These processes produce oligomeric siloxanes and organosilanes containing moisture sensitive propoxy and siloxy-zirconate groups. The obtained
Saravanan Karuppiah et al.
ACS nano, 14(9), 12006-12015 (2020-09-10)
Silicon (Si) is the most promising anode candidate for the next generation of lithium-ion batteries but difficult to cycle due to its poor electronic conductivity and large volume change during cycling. Nanostructured Si-based materials allow high loading and cycling stability
Ahmad Arar et al.
Molecules (Basel, Switzerland), 25(7) (2020-04-05)
Currently, Redox Initiating Systems (RISs) of Free Radical Polymerization (FRP) are mainly based on the interaction of aromatic amines with peroxides (e.g., dibenzoyl peroxide (BPO)) that can be both toxic and unstable. In the present work, we aim to replace
Christopher L Rock et al.
Dalton transactions (Cambridge, England : 2003), 48(2), 461-467 (2018-11-30)
The phosphine-substituted α-diimine Ni precursor, (Ph2PPrDI)Ni, has been found to catalyze alkene hydrosilylation in the presence of Ph2SiH2 with turnover frequencies of up to 124 h-1 at 25 °C (990 h-1 at 60 °C). Moreover, the selective hydrosilylation of allylic
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