scholarly journals Alkaline Earth Complexes of a Sterically Demanding Guanidinate Ligand

2015 ◽  
Vol 2015 (36) ◽  
pp. 5892-5902 ◽  
Author(s):  
Graeme J. Moxey ◽  
Alexander J. Blake ◽  
William Lewis ◽  
Deborah L. Kays
2014 ◽  
Vol 70 (a1) ◽  
pp. C640-C640
Author(s):  
Petra Bombicz ◽  
Ewald Sattler ◽  
Ilona Kovács ◽  
Alexander Rothenberger ◽  
Alexander Okrut

The alkali and alkaline earth phosphanides have already been intensively studied, nonetheless there are only a few reports on the alkali metal diphosphanides, on their structural properties and their synthetic use as building blocks for the synthesis of phosphorus-rich compounds and, in particular, transition- metal complexes. This study extends the so far small family of lithium diphosphanides with the series of Li(L)nP-(SiMe3)-PtBu2, where L = THF, n = 0–3; L = TMEDA or 12-crown-4, n = 2. The coordination numbers of the Li ions are in the range of two to eight in the investigated compounds. There is a clear correlation between the Li-P distance and the coordination number of the Li atom. The higher the coordination number of the Li atom, the longer the Li–P distance is. Coordination numbers of four or higher lead to ionic structures. The influence of the space requirement of the phosphorus substituents on the Li-P bond length should also be taken into account especially in the case of coordination number two. Eight-membered ring structures are realized when the formation of four-membered rings is prevented by sterically demanding substituents. This work is a contribution to the fine tuning of structures by donor molecules and substituents [1].


1976 ◽  
Vol 37 (C7) ◽  
pp. C7-158-C7-158
Author(s):  
A. RASCÓN ◽  
J. L. ALVAREZ RIVAS

2020 ◽  
Author(s):  
Boris Sheludko ◽  
Cristina Castro ◽  
Chaitanya Khalap ◽  
Thomas Emge ◽  
Alan Goldman ◽  
...  

<b>Abstract:</b> The production of olefins via on-purpose dehydrogenation of alkanes allows for a more efficient, selective and lower cost alternative to processes such as steam cracking. Silica-supported pincer-iridium complexes of the form [(≡SiO-<sup>R4</sup>POCOP)Ir(CO)] (<sup>R4</sup>POCOP = κ<sup>3</sup>-C<sub>6</sub>H<sub>3</sub>-2,6-(OPR<sub>2</sub>)<sub>2</sub>) are effective for acceptorless alkane dehydrogenation, and have been shown stable up to 300 °C. However, while solution-phase analogues of such species have demonstrated high regioselectivity for terminal olefin production under transfer dehydrogenation conditions at or below 240 °C, in open systems at 300 °C, regioselectivity under acceptorless dehydrogenation conditions is consistently low. In this work, complexes <a>[(≡SiO-<i><sup>t</sup></i><sup>Bu4</sup>POCOP)Ir(CO)] </a>(<b>1</b>) and [(≡SiO-<i><sup>i</sup></i><sup>Pr4</sup>PCP)Ir(CO)] (<b>2</b>) were synthesized via immobilization of molecular precursors. These complexes were used for gas-phase butane transfer dehydrogenation using increasingly sterically demanding olefins, resulting in observed selectivities of up to 77%. The results indicate that the active site is conserved upon immobilization.


2019 ◽  
Author(s):  
Nga Phung ◽  
Hans Köbler ◽  
Diego Di Girolamo ◽  
Thi Tuyen Ngo ◽  
Gabrielle Sousa e Silva ◽  
...  

2020 ◽  
pp. 25-34
Author(s):  
V. P. Ermakova ◽  
◽  
S. Yu. Melchakov ◽  
V. G. Smirnova ◽  
L. A. Ovchinnikova ◽  
...  

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