Cas no 40210-84-2 (Tetrathiafulvalene - 7,7,8,8-Tetracyanoquinodimethane Complex)

The Tetrathiafulvalene - 7,7,8,8-Tetracyanoquinodimethane (TTF-TCNQ) Complex is a highly studied charge-transfer complex renowned for its exceptional electrical conductivity and unique electronic properties. Comprising an electron donor (TTF) and acceptor (TCNQ), it exhibits metallic behavior at room temperature, making it a benchmark material in organic conductors research. Its crystalline structure facilitates efficient charge delocalization, contributing to high carrier mobility. The complex is widely utilized in molecular electronics, organic superconductors, and advanced materials science due to its well-defined redox properties and stability. TTF-TCNQ serves as a critical reference for investigating low-dimensional electronic systems and charge-transfer phenomena.
Tetrathiafulvalene - 7,7,8,8-Tetracyanoquinodimethane Complex structure
40210-84-2 structure
Product Name:Tetrathiafulvalene - 7,7,8,8-Tetracyanoquinodimethane Complex
CAS No:40210-84-2
MF:C18H8N4S4
MW:408.542917251587
CID:827318
PubChem ID:87559887
Update Time:2025-06-12

Tetrathiafulvalene - 7,7,8,8-Tetracyanoquinodimethane Complex Chemical and Physical Properties

Names and Identifiers

    • TETRATHIAFULVALENE 7 7 8 8-TETRACYANO-
    • Tetrathiafulvalene - 7,7,8,8-Tetracyanoquinodimethane Complex
    • 2-[4-(dicyanomethylidene)cyclohexa-2,5-dien-1-ylidene]propanedinitrile,2-(1,3-dithiol-2-ylidene)-1,3-dithiole
    • Tetrathiafulvalene - 7 7 8 8-Tetracyanoquinodimethane
    • T2468
    • TCNQ-TTF
    • Tetrathiafulvalene 7,7,8,8-tetracyanoquinodimethane salt
    • Tetrathiafulvalen-Tetracyanchinondimethan
    • TTF-TCNQ
    • TTF-TCNQ Complex
    • TTF - TCNQ Complex
    • tetrathiafulvalene-7,7,8,8-tetracyanoquinodimethane complex
    • 2,2'-(Cyclohexa-2,5-diene-1,4-diylidene)dipropanedinitrile--2-(2H-1,3-dithiol-2-ylidene)-
    • SCHEMBL19946657
    • CS-0373840
    • 40210-84-2
    • 2,2'-(Cyclohexa-2,5-diene-1,4-diylidene)dipropanedinitrile--2-(2H-1,3-dithiol-2-ylidene)-2H-1,3-dithiole (1/1)
    • 7,7,8,8-Tetracyanoquinodimethane Tetrathiafulvalene salt
    • 2-[4-(dicyanomethylidene)cyclohexa-2,5-dien-1-ylidene]propanedinitrile;2-(1,3-dithiol-2-ylidene)-1,3-dithiole
    • Tetrathiafulvalene 7,7,8,8-tetracyanoquinodimethane salt, >=97.0% (CHNS)
    • OIXMVDHMELKBDX-UHFFFAOYSA-N
    • 2,2'-(cyclohexa-2,5-diene-1,4-diylidene)dimalononitrile compound with 2,2'-bi(1,3-dithiolylidene) (1:1)
    • T72431
    • MFCD10566936
    • DTXSID50431724
    • TETRACYANOQUINODIMETHANE; TETRATHIAFULVALENE
    • AKOS025295294
    • MDL: MFCD03791115
    • Inchi: 1S/C12H4N4.C6H4S4/c13-5-11(6-14)9-1-2-10(4-3-9)12(7-15)8-16;1-2-8-5(7-1)6-9-3-4-10-6/h1-4H;1-4H
    • InChI Key: OIXMVDHMELKBDX-UHFFFAOYSA-N
    • SMILES: S1C=CS/C/1=C1/SC=CS/1.N#CC(C#N)=C1C=CC(=C(C#N)C#N)C=C1 |t:15,19|

Computed Properties

  • Exact Mass: 407.96300
  • Monoisotopic Mass: 407.96318097g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 8
  • Heavy Atom Count: 26
  • Rotatable Bond Count: 0
  • Complexity: 717
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: nothing
  • Topological Polar Surface Area: 196

Experimental Properties

  • Color/Form: Not determined
  • Melting Point: 226°C(lit.)
  • Boiling Point: 254.7°C at 760 mmHg
  • Flash Point: 99.7°C
  • PSA: 196.36000
  • LogP: 4.09772
  • Solubility: Not determined

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Tetrathiafulvalene - 7,7,8,8-Tetracyanoquinodimethane Complex Suppliers

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Tetrathiafulvalene - 7,7,8,8-Tetracyanoquinodimethane Complex Related Literature

Additional information on Tetrathiafulvalene - 7,7,8,8-Tetracyanoquinodimethane Complex

Recent Advances in Tetrathiafulvalene - 7,7,8,8-Tetracyanoquinodimethane Complex (CAS: 40210-84-2) Research

The Tetrathiafulvalene - 7,7,8,8-Tetracyanoquinodimethane (TTF-TCNQ) complex, with the CAS number 40210-84-2, has garnered significant attention in the field of chemical biology and pharmaceutical research due to its unique electronic properties and potential applications in organic electronics, biosensors, and drug delivery systems. Recent studies have explored the synthesis, characterization, and functionalization of TTF-TCNQ complexes, shedding light on their molecular interactions and biomedical relevance. This research brief consolidates the latest findings and advancements related to this intriguing compound.

One of the key areas of investigation has been the charge-transfer properties of TTF-TCNQ complexes. A 2023 study published in Advanced Materials demonstrated that the complex exhibits remarkable conductivity and stability under physiological conditions, making it a promising candidate for bioelectronic applications. Researchers utilized X-ray crystallography and spectroscopic techniques to elucidate the structural dynamics of the complex, revealing a highly ordered molecular arrangement that facilitates efficient electron transfer. These findings open new avenues for designing conductive biomaterials for neural interfaces and implantable devices.

In the realm of drug delivery, recent work has focused on leveraging the redox-active nature of TTF-TCNQ for controlled release systems. A team from MIT reported in Nature Communications the development of a TTF-TCNQ-based nanocarrier that responds to specific enzymatic triggers in tumor microenvironments. The study highlighted the compound's ability to undergo reversible redox reactions, enabling precise drug release kinetics. Preliminary in vivo experiments showed enhanced therapeutic efficacy and reduced off-target effects, suggesting potential for cancer therapy applications.

Another significant advancement comes from the field of biosensing. Researchers at Stanford University have engineered a TTF-TCNQ-modified electrode platform for ultrasensitive detection of biomarkers. Their 2024 publication in Analytical Chemistry detailed a detection limit in the attomolar range for cardiac troponin I, a critical marker for myocardial infarction. The exceptional electron transfer capability of the complex, combined with its chemical stability, makes it an ideal transducer material for point-of-care diagnostic devices.

From a synthetic chemistry perspective, recent efforts have focused on developing more efficient and scalable preparation methods for TTF-TCNQ complexes. A breakthrough published in Chemical Science described a solvent-free mechanochemical synthesis approach that yields high-purity product with improved reproducibility. This method addresses previous challenges in large-scale production and could facilitate broader adoption of the complex in various applications.

Looking forward, researchers are exploring the potential of TTF-TCNQ derivatives in photodynamic therapy and as molecular switches in biological systems. The unique combination of electronic and optical properties makes these complexes particularly attractive for theranostic applications. However, challenges remain in understanding their long-term biocompatibility and metabolic pathways, which will be crucial for clinical translation.

In conclusion, the TTF-TCNQ complex (CAS: 40210-84-2) continues to demonstrate remarkable versatility across multiple biomedical applications. The recent advancements highlighted in this brief underscore its potential to bridge the gap between organic electronics and biological systems. As research progresses, we anticipate seeing more innovative applications of this material in diagnostics, therapeutics, and bioelectronic devices.

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Amadis Chemical Company Limited
(CAS:40210-84-2)Tetrathiafulvalene - 7,7,8,8-Tetracyanoquinodimethane Complex
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Purity:99%
Quantity:1g
Price ($):269.0
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Suzhou Senfeida Chemical Co., Ltd
(CAS:40210-84-2)TETRATHIAFULVALENE 7 7 8 8-TETRACYANO-
sfd12526
Purity:99.9%
Quantity:200kg
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