Precursor compound for atomic layer deposition (ALD) or chemical vapor deposition (CVD), and ald/cvd method using same
A compound and precursor technology, applied in the field of ALD/CVD process using it, can solve the problem of low film density and achieve the effect of high reactivity and excellent step coverage
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Embodiment 1
[0063] [Example 1] Al(CH 3 ) 2 [CH 3 OC(CH 3 ) 2 CH 2 Preparation of NtBu]
[0064] At -78°C, 1 equivalent of the ligand CH 3 OC(CH 3 ) 2 CH 2 NtBu added to 1 equivalent of 2M Al(Me) in hexane or heptane 3 , after which the temperature was slowly raised to room temperature and stirring was carried out for about 16 hours. The reaction was terminated and the solvent was removed in vacuo. The compound thus obtained was subjected to vacuum distillation, resulting in a colorless liquid precursor Al(CH 3 ) 2 [CH 3 OC(CH 3 ) 2 CH 2 NtBu]. 1 H NMR (C 6 D. 6 ):δ2.75(Al(CH 3 ) 2 [CH 3 OC(CH 3 ) 2 CH 2 NtBu],s,2H),2.63(Al(CH 3 ) 2 [CH 3 OC(CH 3 ) 2 CH 2 NtBu],s,3H),1.28Al(CH 3 ) 2 [CH 3 OC(CH 3 ) 2 CH 2 NtBu],s,9H),0.83(Al(CH 3 ) 2 [CH 3 OC(CH 3 ) 2 CH 2 NtBu],s,6H),-0.43(Al(CH 3 ) 2 [CH 3 OC(CH 3 ) 2 CH 2 NtBu],s,6H).
Embodiment 2
[0065] [Example 2] Al(CH 3 ) 2 [CH 3 OCH (CH 3 )CH 2 Preparation of NtBu]
[0066] At -78°C, 1 equivalent of the ligand CH 3 OCH (CH 3 )CH 2 NtBu added to 1 equivalent of 2M Al(Me) in hexane or heptane 3, after which the temperature was slowly raised to room temperature and stirring was carried out for about 16 hours. The reaction was terminated and the solvent was removed in vacuo. The compound thus obtained was subjected to vacuum distillation, resulting in a colorless liquid precursor Al(CH 3 ) 2 [CH 3 OCH (CH 3 )CH 2 NtBu]. 1 H NMR (C 6 D. 6 ):δ3.40-3.32(Al(CH 3 ) 2 [CH 3 OCH (CH 3 )CH 2 NtBu],m,1H),2.88(Al(CH 3 ) 2 [CH 3 OCH (CH 3 )CH 2 NtBu],dd,J 1 =11.1Hz,J 2 =4.7Hz,1H),2.69-2.65(Al(CH 3 ) 2 [CH 3 OCH (CH 3 )CH 2 NtBu],m,1H),2.66(Al(CH 3 ) 2 [CH 3 OCH (CH 3 )CH 2 NtBu],s,3H),1.29(Al(CH 3 ) 2 [CH 3 OCH (CH 3 )CH 2 NtBu],s,9H),0.68(Al(CH 3 ) 2 [CH 3 OCH (CH 3 )CH 2 NtBu], d, J=5.8Hz, 3H), -0.40(Al(CH 3 ) 2 [CH 3 OCH (CH ...
Embodiment 3
[0067] [Example 3] Al(CH 3 ) 2 [CH 3 OCH 2 CH 2 Preparation of NtBu]
[0068] At -78°C, 1 equivalent of the ligand CH 3 OCH 2 CH 2 NHtBu added to 1 equivalent of 2MAl(Me) in hexane or heptane 3 , after which the temperature was slowly raised to room temperature and stirring was carried out for about 16 hours. The reaction was terminated and the solvent was removed in vacuo. The compound thus obtained was subjected to vacuum distillation, resulting in a colorless liquid precursor Al(CH 3 ) 2 [CH 3 OCH 2 CH 2 NtBu]. 1 H NMR (C 6 D. 6 ):δ3.09(Al(CH 3 ) 2 [CH 3 OCH 2 CH 2 NtBu], t, J=6.9Hz, 2H), 2.79(Al(CH 3 ) 2 [CH 3 OCH 2 CH 2 NtBu], t, J=6.9Hz, 2H), 2.62(Al(CH 3 ) 2 [CH 3 OCH 2 CH 2 NtBu],s,3H),1.28(Al(CH 3 ) 2 [CH 3 OCH 2 CH 2 NtBu],s,9H),-0.44(Al(CH 3 ) 2 [CH 3 OCH 2 CH 2 NtBu],s,6H).
[0069] Here, when M (transition metal) is Zn (zinc), the synthesis process is shown in Scheme 3 below.
[0070] [Option 3]
[0071]
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