产品名称
双(环戊二烯基)二氯化锆(IV), ≥98%
InChI key
QRUYYSPCOGSZGQ-UHFFFAOYSA-L
InChI
1S/2C5H5.2ClH.Zr/c2*1-2-4-5-3-1;;;/h2*1-5H;2*1H;/q;;;;+2/p-2
SMILES string
Cl[Zr]Cl.[CH]1[CH][CH][CH][CH]1.[CH]2[CH][CH][CH][CH]2
assay
≥98%
form
solid
reaction suitability
core: zirconium, reaction type: Polymerization Reactions, reagent type: catalyst
reaction type: Olefin Metathesis
greener alternative product characteristics
Catalysis
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sustainability
Greener Alternative Product
parameter
moisture sensitive
mp
242-245 °C (lit.)
greener alternative category
, Aligned
storage temp.
2-8°C
Quality Level
General description
我们致力于为您提供更环保的替代产品,以符合“绿色化学的12项原则”的一项或多项原则要求。该产品为增强型,提高了催化效率。详细信息见于此处。
二氯二茂锆可用作催化剂,从而实现吡咯的高效催化,产率高,简化纯化过程。
二氯二茂锆可用作催化剂,从而实现吡咯的高效催化,产率高,简化纯化过程。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Wen-Xiong Zhang et al.
Accounts of chemical research, 44(7), 541-551 (2011-05-27)
Characterizing reactive organometallic intermediates is critical for understanding the mechanistic aspects of metal-mediated organic reactions. Moreover, the isolation of reactive organometallic intermediates can often result in the ability to design new synthetic methods. In this Account, we outline synthetic methods
Christine Bibal et al.
Dalton transactions (Cambridge, England : 2003), (21)(21), 2866-2870 (2008-05-15)
A new family of hydroxytris(pentafluorophenyl)borate anions [B(C6F5)3OH](-) associated with organic and aprotic cations c+ (imidazolium, pyrrolidinium and phosphonium) has been prepared by a general one-pot synthesis that implies the chloride borate analogues [B(C6F5)3Cl](-)[c]+. The [c]+[B(C6F5)3OH](-) salts have been isolated and
Andy M Chapman et al.
Journal of the American Chemical Society, 133(45), 18463-18478 (2011-10-01)
The extension of the frustrated Lewis pair (FLP) concept to the transition series with cationic zirconocene-phosphinoaryloxide complexes is demonstrated. Such complexes mimic the reactivity of main group FLPs in reactions such as heterolytic hydrogen cleavage, CO(2) activation, olefin and alkyne
José Barluenga et al.
Organic letters, 9(16), 3081-3084 (2007-07-20)
A new regio- and stereoselective zirconocene-catalyzed reaction for the synthesis of medium-sized rings is described. The global reaction supposes a formal ring expansion of a cyclic enol ether to give a functionalized carbocycle.
Sven Tobisch
Dalton transactions (Cambridge, England : 2003), (35)(35), 4277-4285 (2006-08-26)
The complete sequence of steps of a tentative catalytic cycle for intramolecular hydroamination/cyclisation (IHC) of 4,5-hexadien-1-ylamine (1) by a prototypical cationic [Cp(2)ZrCH(3)](+) zirconocene precatalyst (2) has been examined by employing a gradient-corrected DFT method. The predicted smooth overall reaction energy
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