应用化工
應用化工
응용화공
APPLIED CHEMICAL INDUSTRY
2014年
6期
1042-1046,1049
,共6页
乐传俊%壮亚峰%刘宝亮%苏扬
樂傳俊%壯亞峰%劉寶亮%囌颺
악전준%장아봉%류보량%소양
Ru-BINAP%介孔 γ-Al2 O3%负载化%不对称催化氢化%手性 1,2-丙二醇
Ru-BINAP%介孔 γ-Al2 O3%負載化%不對稱催化氫化%手性 1,2-丙二醇
Ru-BINAP%개공 γ-Al2 O3%부재화%불대칭최화경화%수성 1,2-병이순
Ru-BINAP%mesoporous γ-Al2 O3%loading%catalytic asymmetric hydrogenation%chiral 1,2-propanediol
利用电荷作用负载法,使离子型[RuCl((R)-BINAP)(p-cymene)]+ Cl -配合物负载于介孔γ-Al2 O3上,获得了羟基丙酮不对称加氢催化剂。考察了溶剂、温度和氢气压力等对羟基丙酮催化加氢反应的影响。结果表明,[Ru]配合物能够负载于介孔γ-Al2 O3上(Ru 质量含量为3.6%),且催化剂主要位于γ-Al2 O3表面曲度大的位置,催化剂结构在负载前后没有发生变化,具有催化反应中的热稳定性。在60℃、24 h、氢气压力8 MPa 和10 mL 甲醇作为溶剂的反应条件,58.5 mg 催化剂催化2 mL 羟基丙酮不对称加氢反应,获得了63.6%的催化转化率和42.6%的对映体选择性。
利用電荷作用負載法,使離子型[RuCl((R)-BINAP)(p-cymene)]+ Cl -配閤物負載于介孔γ-Al2 O3上,穫得瞭羥基丙酮不對稱加氫催化劑。攷察瞭溶劑、溫度和氫氣壓力等對羥基丙酮催化加氫反應的影響。結果錶明,[Ru]配閤物能夠負載于介孔γ-Al2 O3上(Ru 質量含量為3.6%),且催化劑主要位于γ-Al2 O3錶麵麯度大的位置,催化劑結構在負載前後沒有髮生變化,具有催化反應中的熱穩定性。在60℃、24 h、氫氣壓力8 MPa 和10 mL 甲醇作為溶劑的反應條件,58.5 mg 催化劑催化2 mL 羥基丙酮不對稱加氫反應,穫得瞭63.6%的催化轉化率和42.6%的對映體選擇性。
이용전하작용부재법,사리자형[RuCl((R)-BINAP)(p-cymene)]+ Cl -배합물부재우개공γ-Al2 O3상,획득료간기병동불대칭가경최화제。고찰료용제、온도화경기압력등대간기병동최화가경반응적영향。결과표명,[Ru]배합물능구부재우개공γ-Al2 O3상(Ru 질량함량위3.6%),차최화제주요위우γ-Al2 O3표면곡도대적위치,최화제결구재부재전후몰유발생변화,구유최화반응중적열은정성。재60℃、24 h、경기압력8 MPa 화10 mL 갑순작위용제적반응조건,58.5 mg 최화제최화2 mL 간기병동불대칭가경반응,획득료63.6%적최화전화솔화42.6%적대영체선택성。
Cationic[ RuCl(( R)-BINAP)( p-cymene)]+ Cl - supported by mesoporous γ-Al2 O3 in the charge adsorption method was prepared as a catalyst for the catalytic asymmetric hydrogenation of acetol. The effect of the solvent,temperature and hydrogen pressure on the catalytic activity and the enantiomer selectivity of product was investigated. The results showed that[Ru]complex was successfully loaded on mesoporous γ-Al2 O3(Ru mass content was 3. 6% ),and the catalyst was mainly located in the big curva-ture position of γ-Al2 O3 surface,the structure of the catalyst did not change before and after loading,pres-enting the thermal stability in the catalytic reaction. Under the optimal reactions of the catalyst of 58. 5 mg,the acetol of 2 mL,the reaction temperature of 60 ℃,the hydrogen pressure of 8 MPa,the reac-tion time of 24 h and 10 mL methanol as solvent,the conversion and the enantiomer selectivity to chiral 1, 2-propanediol reached 63. 6% and 42. 6% ,respectively.