首页--数理科学和化学论文--化学论文--有机化学论文

手性多环芳烃

摘要第3-7页
abstract第7-8页
CHAPTER1 INTRODUCTION第11-35页
    1.1 CHIRALITY AND STEREOCHEMISTRY第11-16页
        1.1.1 OPTICAL ACTIVITY第11-12页
        1.1.2 MOLECULAR CHIRALITY AND SPONTANEOUS RESOLUTION第12-13页
        1.1.3 CAHN–INGOLD–PRELOG PRIORITY RULES AND ITS LIMITATION第13-15页
        1.1.4 QUANTIFY CHIRALITY第15-16页
    1.2.POLYAROMATIC HYDROCARBONS第16-25页
        1.2.1 GRAPHENE第17-18页
        1.2.2 CARBON NANOTUBES第18-19页
        1.2.3 CORANNULENE第19-25页
    1.3.CHIRAL POLYCYCLIC AROMATIC HYDROCARBONS第25-31页
        1.3.1 RESOLVED CHIRAL POLYCYCLIC AROMATIC HYDROCARBONS第26-29页
        1.3.2 UNRESOLVED CHIRAL POLYCYCLIC AROMATIC HYDROCARBONS第29-31页
    1.4.CORANNULENE-BASED SKELETALLY CHIRALΠ-SYSTEMS第31-35页
        1.4.1.BICORANNULENYL第31-32页
        1.4.2.CYCLOTRIMERIZATION OF CORANNULENE第32-35页
CHAPTER2 THE PROJECT-MOTIVATION AND GOALS OF THE THESIS第35-37页
CHAPTER3 RESULTS AND DISCUSSION第37-87页
    3.1.SYNTHESIS CHIRAL INDENOCORANNULENES第37-43页
        3.1.1.SYNTHESIS OF MONOIODOCORANNULENE第37-38页
        3.1.2.SYNTHESIS OF FLUOROPHENYLDIOXABOROLANE DERIVATIVES第38-39页
        3.1.3.SYNTHESIS OF C-F AND C-CL ACTIVATION PRECURSORS第39-40页
        3.1.4.SYNTHESIS OF INDENOCORANNULENES VIA C-F METHODS第40-42页
        3.1.5.SYNTHESIS OF INDENOCORANNULENES VIA C-CL METHODS第42-43页
    3.2.PHOTOPHYSICAL MEASUREMENTS第43-45页
    3.3.RESOLUTION OF CHIRAL INDENOCORANNULENES第45-60页
        3.3.1 ANALYTICAL CHIRAL HPLC SEPARATION FOR COMPOUND1A第46-47页
        3.3.2 SEMI-PREPARATIVE SEPARATION FOR COMPOUND1A第47-48页
        3.3.3 ANALYTICAL CHIRAL HPLC SEPARATION FOR COMPOUND1B第48-49页
        3.3.4 SEMI-PREPARATIVE SEPARATION FOR COMPOUND1B第49-50页
        3.3.5 ANALYTICAL CHIRAL HPLC SEPARATION FOR COMPOUND1C第50-51页
        3.3.6 SEMI-PREPARATIVE SEPARATION FOR COMPOUND1C第51-52页
        3.3.7 ANALYTICAL CHIRAL HPLC SEPARATION FOR COMPOUND1D第52-53页
        3.3.8 SEMI-PREPARATIVE SEPARATION FOR COMPOUND1D第53-55页
        3.3.9 ANALYTICAL CHIRAL HPLC SEPARATION FOR COMPOUND1E第55-56页
        3.3.10 SEMI-PREPARATIVE SEPARATION FOR COMPOUND1E第56-57页
        3.3.11 ANALYTICAL CHIRAL HPLC SEPARATION FOR COMPOUND1F第57-58页
        3.3.12 SEMI-PREPARATIVE SEPARATION FOR COMPOUND1F第58-60页
    3.4.KINETIC STUDIES OF RACEMIZATION第60-76页
        3.4.1.KINETIC OF1A ENANTIOMERIZATION第60-71页
        3.4.2.KINETIC OF1B ENANTIOMERIZATION第71-72页
        3.4.3.KINETIC OF1C ENANTIOMERIZATION第72-73页
        3.4.4.KINETIC OF1D ENANTIOMERIZATION第73-74页
        3.4.5.KINETIC OF1E ENANTIOMERIZATION第74-75页
        3.4.6.KINETIC OF1F ENANTIOMERIZATION第75-76页
    3.5.HIGH-ORDER EFFECTS FOR TWO SPIN SYSTEMS第76-79页
    3.6.OPTICAL PROPERTIES OF CHIRAL INDENOCORANNULENES第79-84页
        3.6.1.INTRODUCTION第79-80页
        3.6.2.OPTICAL ROTATIONS第80-82页
        3.6.3.ELECTRON CIRCULAR DICHROISM第82-83页
        3.6.4.VIBRATIONAL CIRCULAR DICHROISM第83-84页
    3.7.SINGLE CRYSTAL第84-87页
CHAPTER4 CONCLUSION AND OUTLOOK第87-91页
CHAPTER5 EXPERIMENTAL PART第91-139页
    5.1.GENERAL INFORMATION第91-92页
    5.2.SYNTHESIS AND CHARACTERIZATION第92-109页
    5.3.NMR SPECTRA第109-123页
    5.4.ECD SPECTRA第123-129页
    5.5.VCD SPECTRA第129-136页
    5.6.SINGLE CRYSTAL第136-137页
    5.7.COMPUTATIONAL METHODS第137-139页
REFERENCES第139-147页
Publications and participation in scientific research第147-149页
Acknowledgement第149页

论文共149页,点击 下载论文
上一篇:我国A股上市公司零杠杆策略与企业绩效相关性研究
下一篇:高水热稳定性氨基功能化硅胶色谱填料:制备、评价与应用