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Download 1, 1-binaphthyl-based Chiral Materials: Our Journey by Lin Pu PDF

By Lin Pu

Chiral fabrics were studied within the division of Chemistry on the collage of Virginia for functions in components like uneven catalysis, enantioselective fluorescent sensing, and optical/electrical fabrics. Optically lively 1,1 -binaphthyl molecules are used to construct novel chiral polymers, dendrimers, macrocycles, and acyclic molecules. 1,1 -Binaphthyl molecules are selected due to their remarkably reliable chiral configuration in addition to their excessive uneven inductions in lots of methods. during this e-book, either the elemental wisdom in regards to the 1,1 -binaphthyl molecules and the synthesis of the structurally assorted 1,1 -binaphthyl-based fabrics are defined. The functions of those fabrics in a number of fields also are mentioned. This booklet will function a reference for graduate scholars in addition to different execs operating within the similar fields. advent approximately 1,1 -Binaphthyls major Chain Chiral-Conjugated Polymers Polybinaphthyls in uneven Catalysis uneven Catalysis by means of BINOL and Its Non-Polymeric Derivatives Enantioselective Fluorescent Sensors in line with 1,1 -Binaphthyl Derived Dendrimers, Small Molecules and Macrocycles Miscellaneous experiences on fabrics relating to 1,1 -Binaphthyls

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Extra resources for 1, 1-binaphthyl-based Chiral Materials: Our Journey

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24 is very soluble. 29 as a red solid in 94% yield. 6). 25 has low solubility in organic solvents. 30 as a dark red solid in 54% yield. The lower yield is attributed to the formation of insoluble and probably higher molecular weight materials. 6). 30 are soluble in common organic solvents. They give well-resolved 1 H and 13 C NMR spectra consistent with the expected structures. 6 gives the UV absorptions of the oligothiophenes. 21 S Br AcOH S S R1 S or NBS Br S Br 1. 23b: R = C18H37 Br2, HBr (48%) Mg S S S S S R1 NiCl2(dppp) Br S S NBS (2 eq) 2.

5 is observed at λmax = 328 nm. While excited at 328 nm, it emits at 387 and 405 nm. 5. 11. 6. 11). This polymer is also soluble in common organic solvents. 4). 22, CH2 Cl2 ). 6 loses its hexyl groups from 396 to 478◦ C. After the loss of the hexyl groups, this polymer becomes very stable. It shows no significant mass loss from 480 up to 800◦ C. 5. The UV absorption of this polymer in methylene chloride solution is observed at λmax = 334 nm. 6 gives the same UV absorption as the solution, indicating a minimum interchain π–π interaction in the solid state.

51/Al is prepared by spin-coating the polymer film (∼50 nm) on ITO glass followed by vacuum deposition of Al. This device shows light emission at λ = 554 nm with a shoulder at 500 nm when a positive voltage is applied on the ITO glass of the single-layer device. Thus, the electroluminescence of this device should be predominately from the excimer emission. 0 V. 15% relatively independent of the current. The luminescence of the device is 3200 cd/m2 at 8 mA, corresponding to a current density of 114 mA/cm2 .

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