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Record W2062992725 · doi:10.1021/ic701643d

Multiple Pathways for Dinitrogen Activation during the Reduction of an Fe Bis(iminepyridine) Complex

2008· article· en· W2062992725 on OpenAlex

Why this work is in the frame

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

affAt least one author lists a Canadian institution in the pinned OpenAlex snapshot.

Bibliographic record

VenueInorganic Chemistry · 2008
Typearticle
Languageen
FieldChemistry
TopicOrganometallic Complex Synthesis and Catalysis
Canadian institutionsUniversity of ManitobaUniversity of Ottawa
Fundersnot available
KeywordsChemistryDeprotonationLigand (biochemistry)Medicinal chemistryImineAlkali metalStereochemistryCrystallographyIonOrganic chemistryCatalysis

Abstract

fetched live from OpenAlex

Reduction of the bis(iminopyridine) FeCl(2) complex {2,6-[2,6-(iPr)(2)PhN=C(CH(3))](2)(C(5)H(3)N)}FeCl(2) using NaH has led to the formation of a surprising variety of structures depending on the amount of reductant. Some of the species reported in this work were isolated from the same reaction mixture, and their structures suggest the presence of multiple pathways for dinitrogen activation. The reaction with 3 equiv of NaH afforded {2-[2,6-(iPr)(2)PhN=C(CH(3))]-6-[2,6-(iPr)(20PhN-C=CH(2)](C(5)H(3)N)}Fe(micro,eta(2)-N(2))Na (THF) (1) containing one N(2) unit terminally bound to Fe and side-on attached to the Na atom. In the process, one of the two imine methyl groups has been deprotonated, transforming the neutral ligand into the corresponding monoanionic version. When 4 equiv were employed, two other dinitrogen complexes {2-[2,6-(iPr)(2)PhN=C(CH(3))]-6-[2,6-(iPr)(2)PhN-C=CH(2)](C(5)H(3)N)}Fe(micro-N2)Na(Et(2)O)(3) (2) and {2,6-[2,6-(iPr)(2)PhN=C(CH(3))](2)(C(5)H(3)N)}Fe(micro-N(2))Na[Na(THF)(2)] (3) were obtained from the same reaction mixture. Complex 2 is chemically equivalent to 1, the different degree of solvation of the alkali cation being the factor apparently responsible for the sigma-bonding mode of ligation of the N(2) unit to Na, versus the pi-bonding mode featured in 1. In complex 3, the ligand remains neutral but a larger extent of reduction has been obtained, as indicated by the presence of two Na atoms in the structure. A further increase in the amount of reductant (12 equiv) afforded a mixture of {2-[2,6-(iPr)(2)PhN=C(CH(3))]-6-[2,6-(iPr)(2)PhN-C=CH(2)](C(5)H(3)N)}Fe-N(2) (4) and [{2,6-[2,6-(iPr)(2)PhN=C(CH(3))](2)(C(5)H(3)N)}Fe-N(2)](2)(micro-Na) [Na(THF)(2)](2) (5) which were isolated by fractional crystallization. Complex 4, also containing a terminally bonded N(2) unit and a deprotonated anionic ligand bearing no Na cations, appears to be the precursor of 1. The apparent contradiction that excess NaH is required for its successful isolation (4 is the least reduced complex of this series) is most likely explained by the formation of the partner product 5, which may tentatively be regarded as the result of aggregation between 1 and 3 (with the ligand system in its neutral form). Finally, reduction carried out in the presence of additional free ligand afforded {2,6-[2,6-(iPr)(2)PhN=C(CH(3))](2)(C(5)H(3)N)}Fe(eta(1)-N(2)){2,6-[2,6-(iPr)(2)PhN=C(CH(3))](20(NC(5)H(2))}[Na(THF)(2)] (6) and {2,6-[2,6-(iPr)(2)PhN=C(CH(3))](2)(C(5)H(3)N)}Fe{2,6-[2,6-(iPr)(2)PhN=C(CH(3))](2)(NC(5)H(2))}Na(THF)(2)) (7). In both species, the Fe metal is bonded to the pyridine ring para position of an additional (L)Na unit. Complex 6 chemically differs from 7 (the major component) only for the presence of an end-on coordinated N(2).

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.

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesInsufficient payload (model declined to judge)
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 score0.004
Threshold uncertainty score0.997

Codex and Gemma teacher scores by category

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)0.0040.000

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 head0.036
GPT teacher head0.221
Teacher spread0.185 · 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