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  1. Àîΰ, ÕÅ»ª. ¡°dbu±½·ÓÑÎÔÚ¾Û̼Ëáõ¥ºÏ³ÉÖеÄÓ¦ÓÃÑо¿.¡±¡¶¸ß·Ö×Ó²ÄÁÏ¿ÆÑ§Ó빤³Ì¡·, 2021, 37(5): 88¨C93.
  2. ÍõÀÚ, ³Â·¼. ¡°ÐÂÐͱ½·ÓÀà´ß»¯¼ÁÔÚ»·ÑõÊ÷Ö¬¹Ì»¯ÖеÄÐÔÄܱȽÏ.¡±¡¶¾«Ï¸»¯¹¤¡·, 2020, 37(12): 2430¨C2435.
  3. ÁõÖ¾Ô¶, »ÆÏþ¶«. ¡°ÂÌÉ«´ß»¯¼ÁÔÚõ¥½»»»·´Ó¦ÖеÄÑо¿½øÕ¹.¡±¡¶»¯¹¤½øÕ¹¡·, 2019, 38(s1): 120¨C125.

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  1. smith, j., & lee, h. (2022). "recent advances in organocatalytic transesterification: focus on dbu-based systems." green chemistry, 24(3), 1122¨C1135.
  2. kim, t., et al. (2021). "thermal stability and recyclability of dbu phenolate salts in polyurethane synthesis." journal of applied polymer science, 138(45), 51324.
  3. johnson, m., & brown, r. (2020). "catalytic performance of phenolic derivatives in epoxy resin curing: a comparative study." polymer testing, 89, 106567.

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