Preparation and Structures of Group 12 and 14 Element Halide–Carbene Complexes

2013 ◽  
Vol 66 (10) ◽  
pp. 1235 ◽  
Author(s):  
S. M. Ibrahim Al-Rafia ◽  
Paul A. Lummis ◽  
Anindya K. Swarnakar ◽  
Kelsey C. Deutsch ◽  
Michael J. Ferguson ◽  
...  

The synthesis of a series of N-heterocyclic carbene (NHC) complexes involving zinc, cadmium, and the heavy Group 14 elements germanium, tin, and lead is reported. The direct reaction between the bulky carbene IPr (IPr = (HCNDipp)2C:, Dipp = 2,6-iPr2C6H3) and the Group 14 halide reagents GeCl4 and SnCl4 afforded the 1 : 1 complexes IPr·ECl4 (E = Ge and Sn) in high yield; similarly, ZnI2 interacted with IPr in THF to give the THF-bound complex IPr·ZnI2·THF. CdCl2 underwent divergent chemistry with IPr and the major product isolated was the imidazolium salt [IPrH][IPr·CdCl3], which could be converted into IPr·CdCl2·THF upon treatment with Tl[OTf]. In addition, the stable PbII amide adduct, IPr·PbBr(NHDipp), was prepared. Each of the new carbene–element halide adducts was treated with the hydride sources Li[BH4] and Li[HBEt3] in order to potentially access new element hydride adducts and/or clusters. In most instances scission of the element–carbene bonds transpired, except in the case of IPr·ZnI2·THF, which reacted with two equivalents of Li[BH4] to yield the thermally stable bis(borohydride) zinc complex IPr·Zn(BH4)2.

2009 ◽  
Vol 15 (34) ◽  
pp. 8480-8484 ◽  
Author(s):  
James Y. Becker ◽  
Vladimir Ya. Lee ◽  
Masaaki Nakamoto ◽  
Akira Sekiguchi ◽  
Anna Chrostowska ◽  
...  

2016 ◽  
Vol 18 (26) ◽  
pp. 17750-17756 ◽  
Author(s):  
V. Pershina

Relativistic periodic calculations of adsorption energies of group-12 elements Hg and Cn and group-14 elements Pb and Fl on a hydroxylated (001) α-quartz surface at different adsorbate coverage have been performed using the ADF-BAND program.


2005 ◽  
pp. 5190 ◽  
Author(s):  
Takeaki Iwamoto ◽  
Takashi Abe ◽  
Chizuko Kabuto ◽  
Mitsuo Kira

2019 ◽  
Vol 10 (46) ◽  
pp. 10687-10697 ◽  
Author(s):  
Kyohei Matsuo ◽  
Takuma Yasuda

Blue thermally activated delayed fluorescence emitters incorporating phenazasiline and phenazagermine as donor units are developed, and their structural, photophysical, and electroluminescent properties are systematically investigated.


Polymers ◽  
2021 ◽  
Vol 13 (14) ◽  
pp. 2356
Author(s):  
Marta Navarro ◽  
Andrés Garcés ◽  
Luis F. Sánchez-Barba ◽  
Felipe de la Cruz-Martínez ◽  
Juan Fernández-Baeza ◽  
...  

The direct reaction of the highly sterically demanding acetamidinate-based NNN′-scorpionate protioligand Hphbptamd [Hphbptamd = N,N′-di-p-tolylbis(3,5-di-tertbutylpyrazole-1-yl)acetamidine] with one equiv. of ZnMe2 proceeds in high yield to the mononuclear alkyl zinc complex [ZnMe(κ3-phbptamd)] (1). Alternatively, the treatment of the corresponding lithium precursor [Li(phbptamd)(THF)] with ZnCl2 yielded the halide complex [ZnCl(κ3-phbptamd)] (2). The X-ray crystal structure of 1 confirmed unambiguously a mononuclear entity in these complexes, with the zinc centre arranged with a pseudotetrahedral environment and the scorpionate ligand in a κ3-coordination mode. Interestingly, the inexpensive, low-toxic and easily prepared complexes 1 and 2 resulted in highly efficient catalysts for the ring-opening polymerisation of lactides, a sustainable bio-resourced process industrially demanded. Thus, complex 1 behaved as a single-component robust initiator for the living and immortal ROP of rac-lactide under very mild conditions after a few hours, reaching a TOF value up to 5520 h−1 under bulk conditions. Preliminary kinetic studies revealed apparent zero-order dependence on monomer concentration in the absence of a cocatalyst. The PLA materials produced exhibited narrow dispersity values, good agreement between the experimental Mn values and monomer/benzyl alcohol ratios, as well as enhanced levels of heteroselectivity, reaching Ps values up to 0.74.


2008 ◽  
Vol 27 (13) ◽  
pp. 2915-2917 ◽  
Author(s):  
Anna Chrostowska ◽  
Alain Dargelos ◽  
Alain Graciaa ◽  
Patrick Baylère ◽  
Vladimir Ya. Lee ◽  
...  

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