0000000001299054

AUTHOR

Christopher P. Ender

Oligophenyls with Multiple Disulfide Bridges as Higher Homologues of Dibenzo[c,e][1,2]dithiin: Synthesis and Application in Lithium-Ion Batteries.

Abstract Higher homologues of dibenzo[c,e][1,2]dithiin were synthesized from oligophenyls bearing multiple methylthio groups. Single‐crystal X‐ray analyses revealed their nonplanar structures and helical enantiomers of higher meta‐congener 6. Such dibenzo[1,2]dithiin homologues are demonstrated to be applicable to lithium‐ion batteries as cathode, displaying a high capacity of 118 mAh g−1 at a current density of 50 mA g−1.

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Myrcenol-Based Monomer for Carbanionic Polymerization: Functional Copolymers with Myrcene and Bio-Based Graft Copolymers

A bio-based hydroxyl group-containing diene monomer, silyl-protected β-myrcenol (MyrOSi), is introduced to the field of carbanionic polymerization. Polymerization in cyclohexane, using sec-butyllit...

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Synthesis of Precision Poly(1,3-adamantylene alkylene)s via Acyclic Diene Metathesis Polycondensation

[Image: see text] Fully saturated, aliphatic polymers containing adamantane moieties evenly distributed along the polymer backbone are of great interest due to their exceptional thermal stability, yet more synthetic strategies toward these polymers would be desirable. Herein, we report for the first time the synthesis of poly(1,3-adamantylene alkylene)s based on α,ω-dienes containing bulky 1,3-adamantylene defects precisely located on every 11th, 17th, 19th, and 21st chain carbon via acyclic diene metathesis polycondensation. All saturated polymers revealed excellent thermal stabilities (452–456 °C) that were significantly higher compared to those of structurally similar polyolefins with al…

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CCDC 1910693: Experimental Crystal Structure Determination

Related Article: Christoph Sonnenschein, Christopher P. Ender, Faxing Wang, Dieter Schollmeyer, Xinliang Feng, Akimitsu Narita, Klaus Müllen|2020|Chem.-Eur.J.|26|8007|doi:10.1002/chem.202000728

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CCDC 1910690: Experimental Crystal Structure Determination

Related Article: Christoph Sonnenschein, Christopher P. Ender, Faxing Wang, Dieter Schollmeyer, Xinliang Feng, Akimitsu Narita, Klaus Müllen|2020|Chem.-Eur.J.|26|8007|doi:10.1002/chem.202000728

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CCDC 1910691: Experimental Crystal Structure Determination

Related Article: Christoph Sonnenschein, Christopher P. Ender, Faxing Wang, Dieter Schollmeyer, Xinliang Feng, Akimitsu Narita, Klaus Müllen|2020|Chem.-Eur.J.|26|8007|doi:10.1002/chem.202000728

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CCDC 1910694: Experimental Crystal Structure Determination

Related Article: Christoph Sonnenschein, Christopher P. Ender, Faxing Wang, Dieter Schollmeyer, Xinliang Feng, Akimitsu Narita, Klaus Müllen|2020|Chem.-Eur.J.|26|8007|doi:10.1002/chem.202000728

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CCDC 1910692: Experimental Crystal Structure Determination

Related Article: Christoph Sonnenschein, Christopher P. Ender, Faxing Wang, Dieter Schollmeyer, Xinliang Feng, Akimitsu Narita, Klaus Müllen|2020|Chem.-Eur.J.|26|8007|doi:10.1002/chem.202000728

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CCDC 1910695: Experimental Crystal Structure Determination

Related Article: Christoph Sonnenschein, Christopher P. Ender, Faxing Wang, Dieter Schollmeyer, Xinliang Feng, Akimitsu Narita, Klaus Müllen|2020|Chem.-Eur.J.|26|8007|doi:10.1002/chem.202000728

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CCDC 1910698: Experimental Crystal Structure Determination

Related Article: Christoph Sonnenschein, Christopher P. Ender, Faxing Wang, Dieter Schollmeyer, Xinliang Feng, Akimitsu Narita, Klaus Müllen|2020|Chem.-Eur.J.|26|8007|doi:10.1002/chem.202000728

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CCDC 1910697: Experimental Crystal Structure Determination

Related Article: Christoph Sonnenschein, Christopher P. Ender, Faxing Wang, Dieter Schollmeyer, Xinliang Feng, Akimitsu Narita, Klaus Müllen|2020|Chem.-Eur.J.|26|8007|doi:10.1002/chem.202000728

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CCDC 1910696: Experimental Crystal Structure Determination

Related Article: Christoph Sonnenschein, Christopher P. Ender, Faxing Wang, Dieter Schollmeyer, Xinliang Feng, Akimitsu Narita, Klaus Müllen|2020|Chem.-Eur.J.|26|8007|doi:10.1002/chem.202000728

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