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mCPCN

mCPCN, 1392506-99-8
Product Code M2272A1
Price $231.00 ex. VAT
$ USD

mCPCN, asymmetric bipolar phosphorescent host material

Used to host blue, green, red and white light emitting TADF-OLED devices.

mCPCN, 9-(3-(9H-Carbazol-9-yl)phenyl)-9H-carbazole-3-carbonitrile, is an asymmetric bipolar and high-triplet-energy (ET = 3.03 eV) phosphorescent host material which could be used for hosting blue, green, red and white light emitting TADF-OLED devices.

The incorporation of the simple and small CN group can greatly improve film morphology and device thermal stabilities. Compared to mCP, CN group attached to the 3-position of the carbazole unit in mCPCN is believed to increases the electron affinity to achieve a rather balanced hole–electron injection and transport properties while not altering electronic transition energies and maintaining a high triplet energy.

General Information

CAS number 1392506-99-8
Chemical formula C31H19N3
Molecular weight 433.5 g/mol
Absorption λmax 326, 339 nm (in DCM)
Fluorescence λem 348, 365 nm (in DCM)
HOMO/LUMO HOMO = 5.80 eV, LUMO = 2.24 eV; ET = 3.03 eV [1]
Full name 9-(3-(9H-Carbazol-9-yl)phenyl)-9H-carbazole-3-carbonitrile
Synonyms mCP-CN
Classification / Family Carbazole derivatives, Hole transporting materials, Phosphorescent host materials, OLEDs, TADF materials, Organic electronics

Product Details

Purity Sublimed* >99.0%
Melting point Tm = 222 °C (lit.), Td = 313 °C (5% weight loss), Tg = 97 °C
Colour White Powder

*Sublimation is a technique used to obtain ultra pure-grade chemicals. For more details about sublimation, please refer to the Sublimed Materials for OLED devices page.

Chemical Structure

Chemical structure of mCPCN, CAS 1392506-99-8
Chemical structure of 9-(3-(9H-Carbazol-9-yl)phenyl)-9H-carbazole-3-carbonitrile (mCPCN), CAS 1392506-99-8

Device Structure(s)

Device structure ITO/TAPC (40 nm)/mCP (10 nm)/mCPCN doped with 8 wt% of
FIrpic (20 nm)/DPPS (5 nm)/3TPYMB (45 nm)/LiF (0.5 nm)/Al
(150 nm) [1]
Colour Blue blue light emitting device
Max. Current Efficiency 58.7 cd/A
Max. EQE 26.4%
Max. Power Efficiency 57.6 lm W−1
Device structure ITO/PEDOT:PSS (70 nm)/TAPC (15 nm)/mCP (5 nm)/mCPCN:DMAC­‐TRZ 8 wt.% (20 nm)/DPPS (5 nm)/3TPYMB (45 nm)/LiF (0.5 nm)/Al (150 nm) [2]
Colour Green green light emitting device
Max. Current Efficiency 66.8 cd/A
Max. EQE 26.5%
Max. Power Efficiency 65.6 lm W−1
Device structure ITO/MoO3 (1 nm)/TAPC (40 nm)/mCP (10 nm)/mCPCN doped with 8 wt % of FIrpic (20 nm)/3TPYMB (50 nm)/LiF (1 nm)/Al (150 nm) [3]
Colour Blue blue light emitting device
Max. Current Efficiency 73.4 cd/A
Max. EQE 30.6%
Max. Power Efficiency 67.8 lm W−1
Device structure ITO/MoO3 (1 nm)/TAPC (40 nm)/mCP (10 nm)/mCPCN doped with 8 wt % of MS2 (20 nm)/3TPYMB (50 nm)/LiF (1 nm)/Al (150 nm) [3]
Colour Blue blue light emitting device
Max. Current Efficiency 79.4 cd/A
Max. EQE 30.1%
Max. Power Efficiency 69.3 lm W−1
Device structure ITO/MoO3 (1 nm)/TAPC/mCP (10 nm)/mCPCN doped with Ir(III) dopants 1m (12 wt.%; 20 nm)/3TPYMB/LiF (0.5 nm)/Al (100 nm) [4]
Colour Blue blue light emitting device
Max. Current Efficiency 69.5 cd/A
Max. EQE 27%
Max. Power Efficiency 68.2 lm W−1
Device structure ITO/MoO3 (1 nm)/TAPC/mCP (10 nm)/mCPCN doped with Ir(III) dopants 2m (12 wt.%; 20 nm)/3TPYMB/LiF (0.5 nm)/Al (100 nm) [4]
Colour Bluish-Green bluish-green light emitting device
Max. Current Efficiency 100 cd/A
Max. EQE 30%
Max. Power Efficiency 92 lm W−1
Device structure ITO/MoO3 (1 nm)/TAPC/mCP (10 nm)/mCPCN doped with Ir(III) dopants 3m (12 wt.%; 20 nm)/3TPYMB/LiF (0.5 nm)/Al (100 nm) [4]
Colour Green green light emitting device
Max. Current Efficiency 110.8 cd/A
Max. EQE 31.4%
Max. Power Efficiency 108.7 lm W−1

Pricing

Grade Order Code Quantity Price
Sublimed (>99%) M2272A1 100 mg £210
Sublimed (>99%) M2272A1 250 mg  £420
Sublimed (>99%) M2272A1 500 mg £720
Sublimed (>99%) M2272A1 1 g £1300

MSDS Documentation

mCPCN MSDSmCPCN MSDS sheet

Literature and Reviews

  1. Incorporation of a CN group into mCP: a new bipolar host material for highly efficient blue and white electrophosphorescent devices, M-S. Lin et al., J. Mater. Chem., 22, 16114 (2012); DOI: 10.1039/C2JM32717A.
  2. Versatile Thermally Activated Delayed Fluorescence Emitter for Both Highly Efficient Doped and Non-Doped Organic Light Emitting Devices, W-L. Tsai et al., Chem. Commun., 51, 13662-13665 (2015); DOI: 10.1039/C5CC05022G.
  3. Anomalously Long-Lasting Blue PhOLED Featuring Phenyl-Pyrimidine Cyclometalated Iridium Emitter, M. Sarma et al., Chem., 3 (3), 461-476 (2017); DOI: 10.1016/j.chempr.2017.08.001.
  4. Bis-tridentate Ir(III) Complexes with Nearly Unitary RGB Phosphorescence and Organic Light-Emitting Diodes with External Quantum Efficiency Exceeding 31%, C-Y. Kuei et al., Adv. Mater., 28 (14); 2795-2800 (2016); DOI: 10.1002/adma.201505790.

To the best of our knowledge the information provided here is accurate. However, Ossila assume no liability for the accuracy of this page. The values provided are typical at the time of manufacture and may vary over time and from batch to batch. All products are for laboratory and research and development use only, and may not be used for any other purpose including health care, pharmaceuticals, cosmetics, food or commercial applications.

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