Citation:
	            
		            LIANG  Yun-Xiao, SHANG  Zhen-Feng, XU  Xiu-Fang, ZHAO  Xue-Zhuang. Regioselectivity of 1,3-Butadiene Diels-Alder Cycloaddition to C59XH(X=N, B)[J]. Acta Physico-Chimica Sinica,
							;2008, 24(10): 1811-1816.
						
							doi:
								10.1016/S1872-1508(08)60074-1
						
					
				
					 
				
	        
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	                	The regioselectivity of Diels-Alder cycloaddition of 1,3-butadiene to C59XH (X=N, B) has been studied theoretically by means of the semiempirical AM1 and DFT (B3LYP/6-31G*) methods. The mechanisms of the cycloaddition on some selected 6—6 bonds of C59XH (X=N, B) have been analyzed. For C59NH, the activation energies become lower with the addition site increasingly farther fromthe N atom; however, they are all higher than that of the reaction of 1,3-butadiene with C60. In contrast to C59NH, for the cycloaddition to C59BH, the activation energies corresponding to 2,12/r-and 2,12/f-transition states, in which the addition sites are the nearest ones to the B atom, are the lowest ones,and are lower than that of the reaction of 1,3-butadiene with C60 by over 18 kJ·mol-1, and the products corresponding to these two transition states are the most stable ones. The different electronic natures ofNandB atoms results in different effects on the Diels-Alder reactions of 1,3-butadiene with C59NH and C59BH; the former makes the reactivity of C59NH reduced and the latter makes the reactivity of C59BH enhanced, relative to that of C60.- 
								Keywords:
								
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												C59XH(X=N, B) ,
- Diels-Alder cycloaddition,
- Regioselectivity,
- AM1,
- DFT
 
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