scholarly journals Selective 1,2 addition of polar X‒H bonds to the Ga–P double bond of gallaphosphene L(Cl)GaPGaL

2022 ◽  
Author(s):  
Mahendra K. Sharma ◽  
Christoph Wölper ◽  
Stephan Schulz

Gallaphosphene L(Cl)GaPGaL 1 (L = HC[C(Me)N(2,6-i-Pr2-C6H3)]2) reacts at ambient temperature with a series of polar X−H bonds, i.e. ammonia, primary amines, water, phenol, thiophenol, and selenophenol, selectively with 1,2 addition...

ACS Catalysis ◽  
2020 ◽  
Vol 10 (14) ◽  
pp. 7763-7772 ◽  
Author(s):  
Chao Xie ◽  
Jinliang Song ◽  
Manli Hua ◽  
Yue Hu ◽  
Xin Huang ◽  
...  

SPE Journal ◽  
2019 ◽  
Vol 24 (05) ◽  
pp. 2409-2422 ◽  
Author(s):  
Elsayed Abdelfatah ◽  
Paula Berton ◽  
Robin D. Rogers ◽  
Steven L. Bryant

Summary Steam injection is widely used for bitumen recovery. However, steam is not efficient for shallow or thin reservoirs because of heat loss in the wellbore or to surrounding formations. Numerous alternatives have been proposed, including the addition of solvents and replacement of steam with volatile solvents. Here, we describe a new technology that combines nonvolatile ionic liquids (ILs) and waterflooding for bitumen recovery that can deliver high recovery at ambient temperature. Different ILs were designed for complete dispersal/dissolution of bitumen at ambient temperature. The designed ILs were tested in coreflood experiments with high–grade oil–sand ore from Alberta. Two different scenarios were tested: continuous injection of ILs at different injection rates and injection of a slug of ILs followed by water injection. Different slug volumes were tested at a constant injection rate. After ILs injection, the oil sand was removed from the column, and the remaining bitumen was quantified using a modified Dean–Stark method. Viscosity and solid–content measurements of the recovered samples at breakthrough were conducted. Bitumen recovery by the designed ILs can be thought of as a solution mining process. Tuning the physical and chemical properties of the ILs is the most important aspect of achieving the desired interaction with the oil–sand system. Properties of the designed IL depend on the selected cation and anion, and the strength of their intermolecular interaction. Primary amines mixed with the oleic acid chosen for IL1 form a viscous IL that can recover bitumen, leaving a slight amount of bitumen behind, but a large pressure gradient. Changing the cation to tertiary amines produces significantly less–viscous ILs, which completely recover the bitumen in the oil–sand column. Moreover, the cation can be tailored to significantly minimize the fines (clay) migration and viscosity of the recovered bitumen and to provide compatibility with an aqueous phase. In all cases, these recoveries are significant, compared with the currently used technologies. This work proves that bitumen recovery from oil sand is possible at low temperatures by means of a process analogous to solution mining with the design of the proper ILs, in contrast to viscosity–reduction processes achieved by thermal methods. The properties of these ILs can be tuned for different recovery mechanisms. Thus, this work establishes the basis for developing a new class of in–situ recovery processes with high recovery efficiencies and low environmental impact.


1995 ◽  
Vol 50 (6) ◽  
pp. 982-989 ◽  
Author(s):  
Sven Thiele ◽  
Gerhard Erker ◽  
Cornelia Fritze ◽  
Christian Psiorz ◽  
Roland Fröhlich

Reaction of lithium(neomenthylcyclopentadienid) 3 with dimethyldichlorosilane gives dimethylbis[3-(neomenthyl)cyclopentadienyl]silane 4 regioselectively as a mixture of double bond shift isomers (57% isolated). Deprotonation with 2 equiv. of butyllithium followed by treatment with zirconiumtetrachloride furnished a mixture of the three {dimethylsilylenbis[η5-3-(neomenthyl)cyclopentadienyl][zirconium dichloride diastereomers from which the pure meso-like isomer 6e [p -R (1′S ,3 ′R ,4 ′R),p -S (1′S ,3 ′R ,4 ′R)] was isolated by fractional crystallization. Complex 6 c was characterized by an X-ray crystal structure analysis. Its D 1 - Zr - D 2 angle of 126.8° is very similar as observed in bis(η-cyclopentadienyl) zirconium dichloride (D 1 and D 2 denote the centroids of the cyclopentadienyl rings). The homogeneous 6c/methylalumoxane Ziegler-type catalyst produces polypropylene of low molecular weight (Mη ≈ 670 at ambient temperature). Related catalyst systems may find interesting applications in organic synthesis.


Synthesis ◽  
2019 ◽  
Vol 51 (12) ◽  
pp. 2579-2583 ◽  
Author(s):  
Andrii Gerasov ◽  
Alexander Shivanyuk ◽  
Volodymyr Fetyukhin ◽  
Oleg Lukin

The reactions of t-Boc-protected secondary and primary amines with difluorocarbene generated from trimethylsilyl (fluorosulfonyl)difluoroacetate [Me3SiOC(O)CF2SO2F] (TFDA) in toluene at 110 °C results in the replacement of t-Bu by difluoromethyl in the t-Boc group. This reaction can be carried out in the presence of CH2Br and COOMe moieties in the structure of the protected amine. In the example of a t-Boc-protected amine containing a C=C double bond, replacement of the t-Bu group and/or cyclodifluoropropanation takes place. Difluoromethyl esters are shown to react with primary and secondary amines yielding the corresponding ureas.


1933 ◽  
Vol 8 (5) ◽  
pp. 458-462 ◽  
Author(s):  
Steward Basterfield ◽  
J. W. Tomecko

The ionization constants of seven isoureas have been measured. The values for simple alkyl isoureas increase definitely from methyl to n-propyl, the n-butyl-isourea showing no further increase. Isobutyl-isourea has a decidedly greater constant than the n-butyl compound. Introduction of the phenyl group into ethyl-isourea lowers the value of the constant as would be expected. The presence of a double bond in the radical also produces a similar effect as shown by a comparison of the values for n-propyl- and allyl-isoureas. Cyclohexyl-isourea has a constant slightly higher than those of n-propyl and n-butyl-isoureas. Some comparison with a series of primary amines is made.


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