Primary studyCore evidenceTransport Physics

Construction of a Succinate-Bridged Cd(II)-Based Two-Dimensional Coordination Polymer for Efficient Optoelectronic Device Fabrication and Explosive Sensing Application

Dutta B., Hazra A., Dey A. et al. · Crystal Growth and Design · 2020 · 765-776

2materials
6samples
4synthesis routes
11measurements
105results
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

Compound 1 selectively detects TNP with strong fluorescence quenching, low detection limit, and a large Stern-Volmer quenching constant.

Caveat: Sensing measured in ACN dispersion; real-world aqueous/solid-device sensing is not established here.

771 · Sensing of epNACs · Figures 10-12 · Linked to 4 structured results

Phase AssignmentSupport assessment: High

Bulk compound 1 is phase-pure by PXRD and thermally stable to about 250 deg C after initial lattice-water loss.

Caveat: PXRD claim is qualitative; no refined PXRD residuals reported.

767 · Thermal Stability and Purity · Figures S4-S5 · Linked to 3 structured results

Structure Property LinkSupport assessment: Medium

TNP quenching is attributed to a combined ICT-RET pathway, supported by DFT orbital energies, pi-pi interaction feasibility, spectral overlap, and nonlinear Stern-Volmer behaviour.

Caveat: Mechanism is inferred from spectroscopy and DFT rather than directly observing charge/energy transfer intermediates.

773 · Sensing of epNACs · Figures 12-15 · Linked to 4 structured results

Structure Property LinkSupport assessment: High

The 2D rectangular-grid coordination sheet is assembled into a 3D supramolecular architecture through C-H...pi and pi...pi interactions among dangling 4-nvp ligands.

Caveat: Property linkage to transport is proposed qualitatively by the authors.

767 · Structural Descriptions · Figure 1; Figure S1 · Linked to 3 structured results

Transport MechanismSupport assessment: Medium

At low bias the device is ohmic, while high-bias transport is assigned to SCLC dominated by discrete trapping levels.

Caveat: Assignment is based on power-law analysis of device I-V curves rather than direct trap spectroscopy.

769 · Electrical Characterization · Figure 6 · Linked to 4 structured results

Transport MechanismSupport assessment: High

Compound 1 behaves as a semiconductor-like Schottky device material with conductivity enhanced by light soaking.

Caveat: Electrical data are thin-film device values, not intrinsic single-crystal conductivity; light-row charge-conducting parameters in Table 2 were partly unavailable in the supplied text/render.

773 · Conclusion · Linked to 6 structured results

Material identities

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

MaterialCompositionStructure contextSource
{[Cd(suc)(4-nvp)2].2H2O}n, compound 1C76H66Cd2N4O11; coordination repeat described as {[Cd(suc)(4-nvp)2].2H2O}nCd(II) centres; Cd2 dimers bridged by succinate ligands; distorted octahedral Cd coordination. · Succinate (suc2-) and 4-(1-naphthylvinyl)pyridine (4-nvp).2D · PristineMonoclinic P21/c; 2D rectangular-grid sheet/(4,4) net in the bc plane, extended to a 3D supramolecular architecture by C-H...pi and pi...pi interactions.765 · Abstract
Compound 1 and epNAC DFT model setModel systems: compound 1, NB, 4-NP, 1,3-DNB, 4-NBA, 3,4-DNT, 3,5-DNBA, TNPCd(II) in compound 1 model; none for molecular analytes. · Compound 1 framework plus nitroaromatic analytes modelled for HOMO/LUMO comparison.unknown · Model SystemDFT model set used to rationalise fluorescence quenching via PET/ICT/RET pathways.772 · Sensing of epNACs · Figure 13

Sample register

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

Show 6 sample records
SampleForm and roleProcessing and geometrySource
Compound 1 dispersion in acetonitrile for epNAC sensingresearch_0116__mat__mat_cd_suc_4nvp_cp1Unknown · Target Sample · Pristine Framework1 mg compound 1 dispersed in 5 mL ACN; analytes added as 10^-4 M solutions.Acetonitrile solution/dispersion medium771 · Sensing of epNACs · Figure 10
DFT model of compound 1 and epNAC analytesresearch_0116__mat__mat_compound1_dft_model_setModel · Model System · ModelB3LYP/LANL2DZ calculations; Gaussian 09 cited.S8 · Table S4 · Table S4
As-synthesised bulk compound 1 powder/crystalsresearch_0116__mat__mat_cd_suc_4nvp_cp1Powder · Target Sample · Pristine FrameworkFresh/as-synthesised material; finely ground for PXRD and used in KBr pellet for IR.KBr pellet for IR; finely ground sample for PXRD; freshly prepared compound for TGA.767 · Thermal Stability and Purity · Figure S5
Compound 1 thin film on normal glass for solid-state UV-visresearch_0116__mat__mat_cd_suc_4nvp_cp1Thin Film · Target Sample · Pristine FrameworkStable DMF dispersion used to prepare a thin film on glass for UV-vis/Tauc analysis.Normal glass substrate767 · Optical Characterization · Figure 2
ITO/compound 1/Al sandwich Schottky diode thin-film deviceresearch_0116__mat__mat_cd_suc_4nvp_cp1Thin Film · Target Sample · Pristine FrameworkDMF dispersion spin-coated on ITO, vacuum dried at 75 deg C, Al electrode deposited by vacuum coating.ITO-coated glass substrate with evaporated Al top electrodes · approximately 1 um766-767 · Device Fabrication
Yellow needle-shaped single crystals of compound 1research_0116__mat__mat_cd_suc_4nvp_cp1Single Crystal · Target Sample · Pristine FrameworkLayering synthesis product obtained after 3 days; used for SCXRD.Crystal size 0.112 x 0.101 x 0.097 mm for SCXRD.766 · Synthesis of Compound 1