Primary studyCore evidenceThin Film Device

Chromone-Based Cd(II) Fluorescent Coordination Polymer Fabricated to Study Optoelectronic and Explosive Sensing Properties

Mandal J., Dey A., Sarkar S. et al. · Inorganic Chemistry · 2024 · 4527-4544

7materials
11samples
7synthesis routes
15measurements
118results
6claims and caveats

Evidence map

Open a family to keep every result attached to its sample, method and conditions.

Author interpretations and caveats

Paraphrased for this database from the authors’ stated interpretations — never quoted verbatim — and kept separate from reported measurements.

Application RelevanceSupport assessment: High

All four CPs are fluorescence turn-off sensors for TNP and DNP in aqueous dispersion, with CP2 most selective for TNP by quenching efficiency and Ksv.

Caveat: Sensing is based on laboratory fluorescence titrations; limits of detection are in micromolar range.

4537-4539 · Plausible Mechanism; Conclusions · Figure 13; Table S6 · Linked to 4 structured results

CaveatSupport assessment: Medium

The authors describe the CPs as nonporous and hydrolytically stable due to tight coordination and weak interlayer interactions; no gas-sorption porosity measurement is reported.

Caveat: Nonporosity is stated in the discussion rather than supported by BET or gas sorption data in the extracted documents.

4536 · Sensing · Figures S102-S105 · Linked to 1 structured result

Structure Property LinkSupport assessment: High

CSD4 is the best optoelectronic device among the four according to diode and charge-transport parameters.

Caveat: Best device claim is based on the reported parameter set, not independent replication.

4534 · Electrical Characterization · Tables S4-S5 · Linked to 8 structured results

Structure Property LinkSupport assessment: Medium

The conductance trend 4 > 2 > 3 > 1 is attributed to differences between 3D dicyanamide frameworks and 1D thiocyanate chains, with more inorganic Cd/pseudohalide acceptor parts aiding charge transport.

Caveat: This is the authors' mechanistic interpretation; direct carrier-path mapping was not reported.

4534 · Electrical Characterization · Linked to 4 structured results

Transport MechanismSupport assessment: Medium

Fluorescence quenching is attributed to static quenching at lower analyte concentration, dynamic quenching at higher concentration, inner filter effects, PET and resonance-energy-transfer contributions.

Caveat: Multiple mechanisms are inferred from spectral overlap, DFT levels and lifetime decreases; mechanistic deconvolution is qualitative.

4537-4538 · Plausible Mechanism of Fluorescence Sensing · Figure 14; Table S8 · Linked to 3 structured results

Transport MechanismSupport assessment: High

Thin-film ITO/CP/Al devices based on CP1-CP4 show semiconductor behaviour and nonlinear rectifying Schottky-barrier-diode characteristics; conductivity increases under illumination.

Caveat: Conductivity values are reported for spin-coated thin films; film thickness is approximate for dielectric calculations.

4532 · Electrical Characterization · Figure 6; Table S3 · Linked to 9 structured results

Material identities

Names and aliases are kept exactly within the paper’s own identity model.

MaterialCompositionStructure contextSource
Complex 1; [Cd(L1)(NCS)2.H2O]n[Cd(L1)(NCS)2.H2O]n; empirical formula C18H20CdN4O3S2Cd(II), distorted octahedral CdN4OS environment · L1 = 3-(((2-(diethylamino)ethyl)imino)methyl)-4H-chromen-4-one; thiocyanate1D · PristineMonoclinic P21/n; [Cd(L)(NCS)]+ units bridged by mu1,3-thiocyanato ions in zigzag 1D chains.4529-4530 · Synthesis and Characterization; Structure Description · Scheme 1; Figure 1
Complex 2; [Cd1.5(L1)(N(CN)2)3]n[Cd1.5(L1)(N(CN)2)3]n; empirical formula C44H40Cd3N22O4Cd(II), dinuclear Cd2N10O2 and mononuclear CdN6 coordination environments · L1 = 3-(((2-(diethylamino)ethyl)imino)methyl)-4H-chromen-4-one; dicyanamide3D · PristineMonoclinic P21/c; dicyanamide-bridged 3D architecture.4531 · Structure Description of Compounds 2 and 4 · Figure 3
Complex 3; [Cd(L2)(NCS)2]n[Cd(L2)(NCS)2]n; empirical formula C16H16CdN4O2S2Cd(II), distorted octahedral CdN4OS environment · L2 = 3-(((2-(dimethylamino)ethyl)imino)methyl)-4H-chromen-4-one; thiocyanate1D · PristineMonoclinic P21/c; [Cd(L)(NCS)]+ units bridged through mu1,3-thiocyanato ions in 1D chains along c.4530 · Structure Description of Compounds 1 and 3 · Figure 2
Complex 4; [Cd1.5(L2)(N(CN)2)3]n[Cd1.5(L2)(N(CN)2)3]n; empirical formula C40H32Cd3N22O4Cd(II), mononuclear CdN6 and CdN5O coordination environments · L2 = 3-(((2-(dimethylamino)ethyl)imino)methyl)-4H-chromen-4-one; dicyanamide3D · PristineMonoclinic P21/c; dicyanamide-bridged 3D architecture.4531-4532 · Structure Description of Compounds 2 and 4 · Figure 4
Bare ITO controlITOindium tin oxideunknown · Model SystemBare ITO-coated glass control.S22-S23 · Electrical Characterization · Figure S34; Table S3
Ligand L1 controlC16H20N2O2none · Schiff base ligand L10D · Model SystemDiscrete organic ligand control used for LSD1 device.4539 · Experimental Section
Ligand L2 controlC14H16N2O2none · Schiff base ligand L20D · Model SystemDiscrete organic ligand control used for LSD2 device.4539 · Experimental Section

Sample register

Sample form, processing state and composition status define the context for measurements.

Show 11 sample records
SampleForm and roleProcessing and geometrySource
Complex 1 light-yellow X-ray-quality crystalsresearch_0594__mat__cp1Single Crystal · Target Sample · Pristine FrameworkSlow-evaporated acetonitrile crystals; also used as bulk material for PXRD, TGA, optical and sensing measurements.4540 · Preparation of (1)
Complex 2 light-yellow X-ray-quality crystalsresearch_0594__mat__cp2Single Crystal · Target Sample · Pristine FrameworkSlow-evaporated acetonitrile crystals; also used as bulk material for PXRD, TGA, optical and sensing measurements.4540 · Preparation of (2)
Complex 3 light-yellow X-ray-quality crystalsresearch_0594__mat__cp3Single Crystal · Target Sample · Pristine FrameworkSlow-evaporated acetonitrile crystals; also used as bulk material for PXRD, TGA, optical and sensing measurements.4540 · Preparation of (3)
Complex 4 light-yellow crystalsresearch_0594__mat__cp4Single Crystal · Target Sample · Pristine FrameworkSlow-evaporated acetonitrile crystals; also used as bulk material for PXRD, TGA, optical and sensing measurements.4540 · Preparation of (4)
CSD1 thin-film Schottky device from CP1research_0594__mat__cp1Thin Film · Target Sample · Pristine FrameworkDMF dispersion spin-coated, dried at 80 deg C in vacuum, Al deposited in vacuum.ITO-coated glass with Al top electrode · ~1 um film used in dielectric calculation; Al electrode diameter 1.5 cm; ITO glass 2 cm x 2 cmS20-S24 · Device Fabrication; Electrical Characterization · Figures S31-S33
CSD2 thin-film Schottky device from CP2research_0594__mat__cp2Thin Film · Target Sample · Pristine FrameworkDMF dispersion spin-coated, dried at 80 deg C in vacuum, Al deposited in vacuum.ITO-coated glass with Al top electrode · ~1 um film used in dielectric calculation; Al electrode diameter 1.5 cm; ITO glass 2 cm x 2 cmS20-S24 · Device Fabrication; Electrical Characterization · Figures S31-S33
CSD3 thin-film Schottky device from CP3research_0594__mat__cp3Thin Film · Target Sample · Pristine FrameworkDMF dispersion spin-coated, dried at 80 deg C in vacuum, Al deposited in vacuum.ITO-coated glass with Al top electrode · ~1 um film used in dielectric calculation; Al electrode diameter 1.5 cm; ITO glass 2 cm x 2 cmS20-S24 · Device Fabrication; Electrical Characterization · Figures S31-S33
CSD4 thin-film Schottky device from CP4research_0594__mat__cp4Thin Film · Target Sample · Pristine FrameworkDMF dispersion spin-coated, dried at 80 deg C in vacuum, Al deposited in vacuum.ITO-coated glass with Al top electrode · ~1 um film used in dielectric calculation; Al electrode diameter 1.5 cm; ITO glass 2 cm x 2 cmS20-S24 · Device Fabrication; Electrical Characterization · Figures S31-S33
Bare ITO controlresearch_0594__mat__ito_controlElectrode · Pristine Control · ModelBare ITO measured under dark and light.ITO-coated glassS22-S23 · Electrical Characterization · Figure S34; Table S3
LSD1 ligand-only Schottky-device controlresearch_0594__mat__l1_controlThin Film · Pristine Control · ModelLigand L1 device control measured under dark and light.ITO-coated glass with Al top electrodeS20-S23 · Device Fabrication; Electrical Characterization · Figure S35; Table S3
LSD2 ligand-only Schottky-device controlresearch_0594__mat__l2_controlThin Film · Pristine Control · ModelLigand L2 device control measured under dark and light.ITO-coated glass with Al top electrodeS20-S23 · Device Fabrication; Electrical Characterization · Figure S35; Table S3