Exploiting Nanospace for Asymmetric Catalysis# Confinement of Immobilized, Single-Site Chiral Catalysts Enhances Enantioselectivity

Exploiting Nanospace for Asymmetric Catalysis# Confinement of Immobilized, Single-Site Chiral Catalysts Enhances Enantioselectivity

ID:40070673

大?。?.36 MB

頁數(shù):13頁

時間:2019-07-19

Exploiting Nanospace for Asymmetric Catalysis# Confinement of Immobilized, Single-Site Chiral Catalysts Enhances Enantioselectivity _第1頁
Exploiting Nanospace for Asymmetric Catalysis# Confinement of Immobilized, Single-Site Chiral Catalysts Enhances Enantioselectivity _第2頁
Exploiting Nanospace for Asymmetric Catalysis# Confinement of Immobilized, Single-Site Chiral Catalysts Enhances Enantioselectivity _第3頁
Exploiting Nanospace for Asymmetric Catalysis# Confinement of Immobilized, Single-Site Chiral Catalysts Enhances Enantioselectivity _第4頁
Exploiting Nanospace for Asymmetric Catalysis# Confinement of Immobilized, Single-Site Chiral Catalysts Enhances Enantioselectivity _第5頁
資源描述:

《Exploiting Nanospace for Asymmetric Catalysis# Confinement of Immobilized, Single-Site Chiral Catalysts Enhances Enantioselectivity 》由會員上傳分享,免費在線閱讀,更多相關(guān)內(nèi)容在學(xué)術(shù)論文-天天文庫。

1、ExploitingNanospaceforAsymmetricCatalysis:Con?nementofImmobilized,Single-SiteChiralCatalystsEnhancesEnantioselectivity,,JOHNMEURIGTHOMAS*ANDROBERTRAJA*DepartmentofMaterialsScience,UniversityofCambridge,CambridgeCB23QZ,U.K.,SchoolofChemistry,UniversityofSouthampt

2、on,High?eld,SouthamptonSO171BJ,U.K.RECEIVEDONSEPTEMBER27,2007CONSPECTUSnthemid-1990s,itbecamepossibletopre-Iparehigh-areasilicashavingporediame-terscontrollablyadjustableintherangeca.20-200?.Moreover,theinnerwallsofthesenanoporoussolidscouldbefunctionalizedtoyie

3、ldsingle-site,chiral,catalyticallyactiveorga-nometalliccenters,theprecisestructuresofwhichcouldbedeterminedusinginsituX-rayabsorptionandFTIRandmultinuclearmagicanglespinning(MAS)NMRspectroscopy.Thisapproachopeneduptheprospectofperformingheterogeneousenantiose-le

4、ctiveconversionsinanovelmanner,underthespatialrestrictionsimposedbythenanocavitieswithinwhichthereac-tionsoccur.Inparticular,itsuggestedanalternativemethodforpreparingpharmaceuticallyandagrochemicallyusefulasymmetricproductsbycapitalizingonthenotion,initiallyten

5、tativelyperceived,thatspatialcon?nementofprochiralreac-tants(andtransitionstatesformedatthechiralactivecenter)wouldprovideanaltogethernewmethodofboostingtheenan-tioselectivityoftheanchoredchiralcatalyst.Initially,weanchoredchiralsingle-siteheterogeneouscatalysts

6、tonanoporescovalentlyviaaligandattachedtoPd(II)orRh(I)centers.Later,weemployedamoreconvenientandcheaperelectrostaticmethod,relyinginpartonstronghydrogenbonding.ThisAccountprovidesmanyexamplesoftheseprocesses,encom-passinghydrogenations,oxidations,andaminations.O

7、fparticularnoteisthefacilesynthesisfrommethylbenzoylformateofmethylmandelate,whichisaprecursorinthesynthesisofpemoline,astimulantofthecentralnervoussystem;ourpro-cedureoffersseveralviablemethodsforreducingketocarboxylicacids.Inadditiontorelyingonearlier(synchrot

8、ron-based)insitutechniquesforcharacterizingcatalysts,wehaveconstructedexperimentalproceduresinvolvingroboticallycontrolledcatalyticreactorsthatallowthekineticsofconve

當(dāng)前文檔最多預(yù)覽五頁,下載文檔查看全文

此文檔下載收益歸作者所有

當(dāng)前文檔最多預(yù)覽五頁,下載文檔查看全文
溫馨提示:
1. 部分包含數(shù)學(xué)公式或PPT動畫的文件,查看預(yù)覽時可能會顯示錯亂或異常,文件下載后無此問題,請放心下載。
2. 本文檔由用戶上傳,版權(quán)歸屬用戶,天天文庫負責(zé)整理代發(fā)布。如果您對本文檔版權(quán)有爭議請及時聯(lián)系客服。
3. 下載前請仔細閱讀文檔內(nèi)容,確認文檔內(nèi)容符合您的需求后進行下載,若出現(xiàn)內(nèi)容與標(biāo)題不符可向本站投訴處理。
4. 下載文檔時可能由于網(wǎng)絡(luò)波動等原因無法下載或下載錯誤,付費完成后未能成功下載的用戶請聯(lián)系客服處理。