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Record W10241858

The synthesis and properties of polyether substituted oligothiophenes : a thesis presented in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Chemistry at Massey University, Palmerston North, New Zealand

2003· dissertation· en· W10241858 on OpenAlexvenueno aff
D. Grant

Bibliographic record

VenueHospital administration in Canada · 2003
Typedissertation
Languageen
FieldChemistry
TopicInorganic and Organometallic Chemistry
Canadian institutionsnot available
Fundersnot available
KeywordsDegree (music)Polymer scienceChemistryEngineeringPhysics
DOInot available

Abstract

fetched live from OpenAlex

A number of novel dialkoxystyryl-substituted terthiophenes were synthesised as precursors to form conducting polymers. These compounds contained either crown ethers or polyether chains designed to complex metal cations, and polymerisable terthiophene moieties. Two isomeric cross-linked bis(terthiophene) crown ethers were also synthesised as monomers for conducting polymer synthesis, but could not be investigated further due to their insolubility. The solubility issue was circumvented by the formation of hemicrown compounds, containing two styryl-terthiophene units linked by a polyether chain. Thiophene analogues of the crown ether, open-chain ether, bis(terthiophene) crown ether and hemicrown compounds were also successfully synthesised and characterised. The response of the terthiophene crown compounds, open-chain compounds and hemicrowns to a large range of metal cations was investigated by UV and fluorescence spectroscopy. The results obtained from this work were consistent with complexation based on size-fit and charge density of ions, and with hard-soft-acid-base theory. Chemical polymerisation of the terthiophene crown monomers and open-chain ether terthiophene compounds was carried out using FeCl3. This led to the isolation of dimeric sexithiophene compounds in high yield. Characterisation of the pure sexithiophene derivatives showed that they were the product of regioselective dimerisation, caused by the asymmetric reactivity of the terthiophene-based monomers. This is believed to be due to uneven electron spin-density distribution, and theoretical calculations on the radical cation support this view. Producing dialkoxystyryl-substituted sexithiophenes by this synthetic route gave excellent yields of isomerically-pure product. Chemical oxidation of terthiophene compounds using Cu(ClO4)2 was observed with UV/VIS/NIR spectroscopy. This allowed the observation and identification of absorption bands due to oxidised species. Reduction of these species led to sexithiophene dimers, as seen for chemical polymerisation using FeCl3. Electrochemical polymerisations of the terthiophene, thiophene and sexithiophene compounds were carried out by cyclic voltammetry. Those that formed adherent films were analysed by UV/VIS/NIR spectroscopy in both the neutral and oxidised form. The electrochemical and spectroscopic evidence again pointed to the formation of dimers as the primary product of oxidation from terthiophene-based monomers. The surface morphology of the films was investigated by scanning electron microscopy, and showed a variety of morphologies.

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 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 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 score0.520
Threshold uncertainty score0.875

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)0.0000.000

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 head0.021
GPT teacher head0.203
Teacher spread0.182 · 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 teacher head, 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

Citations0
Published2003
Admission routes1
Has abstractyes

Explore more

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