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Record W4313311857 · doi:10.1002/chem.202203835

Microporous Metal‐Phosphonates with a Novel Orthogonalized Linker and Complementary Guests: Insights for Trivalent Metal Complexes from Divalent Metal Complexes

2022· article· en· W4313311857 on OpenAlexafffund
Martin Glavinović, Justin H. Perras, Benjamin S. Gelfand, Jian‐Bin Lin, Denis M. Spasyuk, Wen Zhou, George K. H. Shimizu

Bibliographic record

VenueChemistry - A European Journal · 2022
Typearticle
Languageen
FieldChemistry
TopicMetal-Organic Frameworks: Synthesis and Applications
Canadian institutionsCanadian Light Source (Canada)University of SaskatchewanUniversity of Calgary
FundersNatural Sciences and Engineering Research Council of CanadaCanada First Research Excellence Fund
KeywordsLinkerPhosphonateChemistryArylMetal-organic frameworkMetalCrystallographyMicroporous materialHydrogen bondMoleculeMetal ions in aqueous solutionAromaticityInorganic chemistryOrganic chemistryAlkylAdsorption

Abstract

fetched live from OpenAlex

Abstract The reliable self‐assembly of microporous metal‐phosphonate materials remains a longstanding challenge. This stems from, generally, more coordination modes for the functional group allowing more dense structures, and stronger bonding driving less crystalline products. Here, a novel orthogonalized aryl‐phosphonate linker, 1,3,5‐tris(4’‐phosphono‐2’,6’‐dimethylphenyl) benzene (H6L3) has been used to direct formation of open frameworks. The peripheral aryl rings of H6L3 are orthogonalized relative to the central aromatic ring giving a tri‐cleft conformation of the linker in which small aromatic molecules can readily associate. When coordinated to magnesium ions, a series of porous crystalline metal‐organic, and hydrogen‐bonded metal‐organic frameworks (MOFs, HMOFs) are formed (CALF‐41 (Mg), HCALF‐42 (Mg), ‐43 (Mg)). While most metal‐organic frameworks are tailored based on choice of metal and linker, here, the network structures are highly dependent on the inclusion and structure of the guest aromatic compounds. Larger guests, and a higher stoichiometry of metal, result in increased solvation of the metal ion, resulting in networks with connectivities increasingly involving hydrogen‐bonds rather than direct phosphonate coordination. Upon thermal activation and aromatic template removal, the materials exhibit surface areas ranging from 400–600 m2/g. Self‐assembly in the absence of aromatic guests yields mixtures of phases, frequently co‐producing a dense 3‐fold interpenetrated structure (1). Interestingly, a series of both more porous (530–900 m2/g), and more robust solids is formed by complexing with trivalent metal ions (Al, Ga, In) with aromatic guest; however, these are only attainable as microcrystalline powders. The polyprotic nature of phosphonate linkers enables structural analogy to the divalent analogues and these are identified as CALF‐41 analogues. Finally, insights to the structural transformations during metal ion desolvation in this family are gained by considering a pair of structurally related Co materials, whose hydrogen‐bonded (HCALF‐44 (Co)) and desolvated (CALF‐44 (Co)) coordination bonded networks were fully structurally characterized.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.001
Threshold uncertainty score0.002

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.028
GPT teacher head0.241
Teacher spread0.213 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations14
Published2022
Admission routes2
Has abstractyes

Explore more

Same venueChemistry - A European JournalSame topicMetal-Organic Frameworks: Synthesis and ApplicationsFrench-language works237,207