eScholarship
metadata only
Amplification of Lanthanide f‑Orbital Differences by Redox Noninnocent Semiquinone Binding
A deeper understanding of the electronic structure of the lanthanides (Ln) is essential to harness their technological applications and enable responsible recovery/separation. Here, an isostructural series of tris(3,5-dimethyl-1-pyrazolyl)borate (Tp*)-supported LnIII adducts of a redox noninnocent 3
Conceptio Open Archive
Analyze & explore related research in Conceptio
Connect this record directly into your research workflow or AI agent. Explore citations across open repositories, query full text, and export structured proof bundles.
This document is indexed with metadata only: full text is not available in the archive for this record. Open the official source ↗
Related documents
- Direct Assembly of Angular 5–5–5 Tricyclic Skeletons via a Rh(III)-Catalyzed C–H Activation/Annulation Cascade#342076
- Skeletal Editing via Diastereoselective Ring Expansion Enables Enantioenriched Tetrasubstituted Δ 3 -Oxepenes#357549
- Synthesis and molecular structure of η3-[(η5-C5Me5)(CO)2Fe-AsPC(SiMe3)2]M(CO)2(η5-C5H5). M = Mo, W: The first complexes featuring η3-Arsaallyl-ligands#492952
- Synthesis of C3-epi-virenose and anomerically activated derivatives#649379
- Diastereoselective synthesis of boron-derivatives of resorcinarenes from amino alcohols and triethylborane#492567
Record · ID 1145717
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Bring this data into your agent: Connect via MCP or API · 20 free credits to start · no card required
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive