Four organic azide compounds (N3 - CH2R, R : CH3, OCH3, COCH3
and CONH2) were synthesized using a new safe method without heat and distillation procedures, and identified
from their IR and H NMR spectra.
Then their thermal stabilities were evaluated from TDSC measured with SC - DSC. As a result, the
TDSC values for N3 - CH2 - R (R : CH3, OCH3, CONH2,
and COCH3) were shown to be 225 ℃, 173 ℃, 157 ℃ and 130 ℃, respectively.
As compared with substituent constants, thermal stabilities were suggested to become low due to
electron withdrawing group. The bond lengths of trigger linkaeges were not affected by substituent
effects.
Ground states and transition states were optimized for four azide compounds and obtained activation energies.
The activation energies increase accompanying an increase in thermal stabilities.
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ÂоݤȤ¹¤ë¥¨¥Í¥ë¥®¡¼Êª¼Á¤È¤·¤Æ4¼ï¤ÎÃÖ´¹Íµ¡¥¢¥¸²½Êª(N3 - CH2R : R¤Ï¥á¥Á¥ë´ð, ¥á¥È¥¥·´ð, ¥¢¥»¥Á¥ë´ð¤ª¤è¤Ó¥¢¥ß¥É´ð)¤òÁª¤Ó, ¤½¤ì¤é¤ò²ÃÇ®¤ä¾øα¤ÎÁàºî¤ò´Þ¤Þ¤Ê¤¤°ÂÁ´¤ËÇÛθ¤·¤¿ÊýË¡¤òÍѤ¤¤Æ¹çÀ®¤·¤¿Ž¡ Ì©Éõ¥»¥ë¡¡-¡¡¼¨º¹ÁöººÇ®Î̬Äê(SC - DSC)¤òÍѤ¤¤ÆǮʬ²ò³«»Ï²¹ÅÙ(TDSC)ɾ²Á¤·¤¿·ë²Ì, TDSC¤ÏÃÖ´¹´ð¤¬¥á¥Á¥ë´ð(225 ¡î), ¥á¥È¥¥·´ð(173 ¡î), ¥¢¥ß¥É´ð(157 ¡î), ¥¢¥»¥Á¥ë´ð(130 ¡î)¤Î½ç¤ËÄã²¼¤·¤¿Ž¡
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