Binding of fullerenes to cadmium sulfide and cadmium selenide surfaces, photoluminescence as a probe of strong, Lewis acidity-driven, surface adduct formation

1993 ◽  
Vol 115 (17) ◽  
pp. 7789-7793 ◽  
Author(s):  
John Zhongju Zhang ◽  
Margret J. Geselbracht ◽  
Arthur B. Ellis

1983 ◽  
Vol 14 (28) ◽  
Author(s):  
A. S. BARANSKI ◽  
W. R. FAWCETT ◽  
K. GATNER ◽  
A. C. MCDONALD ◽  
J. R. MACDONALD ◽  
...  


2013 ◽  
Vol 423-426 ◽  
pp. 467-470
Author(s):  
Ya Hui Zhang ◽  
Xi Cheng ◽  
Qing Wang

Cadmium sulfide and cadmium selenide have been the subject of considerable interest because of their potentialapplications in many fields. In this paper, the synthesis of cadmium sulfide and cadmium selenide nanostructures is described. The Morphologies of as prepared cadmium sulfide and cadmium selenide nanostructures are summarized. And the applications and prospects of cadmium sulfide and cadmium selenide in this field also are analyzed.



2006 ◽  
Vol 61 (3) ◽  
pp. 265-274 ◽  
Author(s):  
Klaus Knabel ◽  
Heinrich Nöth ◽  
Robert T. Paine

AbstractWhile the diphosphadiboretane (tBuP=Btmp)2, 1, reacts with boron trihalides BX3 (X = Cl, Br, I) with BN cleavage producing a number of unidentifiable products, a new tricyclic BP ring system 2, containing B3P3, PB2C2 and C6 rings, results from the combination of PhBCl2 and 1. B-Chlorocatecholborane and 1 give access to the diborylphosphane 3, tmpBCl-PtBu-cat (cat = C6H4O2B). This shows that the selectivity of the reactions increases as the Lewis acidity of boron halide decreases. The structure of compounds 2 and 3 were determined by X-ray structure analysis. The bicyclic (tmpBP)2 4 forms no adducts with MeI, CF3SO2Me or Ph3C(SnCl5). However, it adds B(C6F5)3 to give 10, the first BX3 adduct of this bicycle that is fully characterized including its molecular structure.



1976 ◽  
Vol 29 (11) ◽  
pp. 2405 ◽  
Author(s):  
Y Farhangi ◽  
DP Graddon

Thermodynamic data are reported for the reaction of Lewis bases with mercury(11) thiocyanate in acetonitrile solution. Pyridine, 4-methylpyridine and tetrahydrothiophen form 1 : 1 adducts with adduct formation constants and enthalpies of formation comparable to those with mercury(11) iodide. 1,l0-Phenanthroline, 2,2'-bipyridine and N,N,N',N?-tetramethylethane-1,2-diamine form chelate 1 : 1 adducts, but with enthalpies of formation little larger than that with pyridine. The phosphines, PPh3 and Pbu3, form 1 : 1 and 1 : 2 adducts of much greater stability, though the enthalpies of formation of these adducts are also similar to that with pyridine; Hg(SCN)2PBu3 is dimeric in dilute solution.



1974 ◽  
Vol 17 (7) ◽  
pp. 1016-1017
Author(s):  
N. G. Gasanov ◽  
Kh. A. Magomedov ◽  
M. A. Magomedov


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