Sodium
superionic conductor (NASICON)-type electrolytes with high
ionic conductivity and moisture/air stability are essential for solid-state
batteries. However, they generally suffer from poor electrochemical
stability and insufficient contact against Li metal, causing severe
performance degradation. To address this challenge, an ionic conductive
metal–organic framework (MOF)-incorporated polymeric layer
(denoted as ZCPL) is prepared and used as the coating layer of Li1.5Al0.5Ge1.5(PO4)3 (LAGP). As a protective layer, ZCPL can effectively prevent the
redox reaciton between LAGP and Li metal, eliminating the formation
of detrimental interphases and cracks upon battery cycling. The adhesive
ZCPL can also infiltrate into the void/gaps of the LAGP surface, generating
a firm connection with intimate contact. Besides, ZCPL with good ionic
conductivity and a soft texture provides rich pathways for fast Li+ transport and ensures a uniform Li+ flow through
the interface. Benefiting from ZCPL, both the Li symmerical cell and
Li/LiFePO4 full cell show long-term cycling stability.
Among the famous Daphniphyllum alkaloids
family,
the calyciphylline A-type subfamily has triggered particular interest
from the organic synthesis community in recent years. Here, we report
divergent total syntheses of three calyciphylline A-type alkaloids,
namely, (−)-10-deoxydaphnipaxianine A, (+)-daphlongamine E,
and (+)-calyciphylline R. Our work highlights an efficient, divergent
strategy via late-stage divinyl carbinol rearrangements, including
an unprecedented oxidative Nazarov electrocyclization using an unfunctionalized
tertiary divinyl carbinol and an unusual allylic alcohol rearrangement.
A highly efficient “donor–acceptor” platinum
catalyst was used for a critical nitrile hydration step. Moreover,
the power of selective amide reductions has also been showcased by
novel and classic tactics.
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