1,1'-[4,8-Bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b']dithiophene-2,6-diyl]bis[1,1,1-trimethylstannane]

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Names

[ Name ]:
1,1'-[4,8-Bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b']dithiophene-2,6-diyl]bis[1,1,1-trimethylstannane]

[Synonym ]:
Stannane, 1,1'-[4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b']dithiene-2,6-diyl]bis[1,1,1-trimethyl-
{4,8-Bis[(2-ethylhexyl)oxy]thieno[2,3-f][1]benzothiene-2,6-diyl}bis(trimethylstannane)
2,6-Bis(trimethyltin)-4,8-bis(2-ethylhexyloxy)benzo[1,2-b:4,5-b']dithiophene
2,6-Bis(trimethylstannyl)-4,8-bis(2-ethylhexyloxy)benzo[1,2-b:4,5-b']dithiophene
[4,8-bis(2-ethylhexoxy)-2-trimethylstannylthieno[2,3-f][1]benzothiol-6-yl]-trimethylstannane
1,1'-[4,8-Bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b']dithiophene-2,6-diyl]bis[1,1,1-trimethylstannane]

Chemical & Physical Properties

[ Boiling Point ]:
665.1±65.0 °C at 760 mmHg

[ Melting Point ]:
75 °C

[ Molecular Formula ]:
C₃₂H₆₀O₂S₂Sn₂

[ Molecular Weight ]:
772.320

[ Flash Point ]:
356.0±34.3 °C

[ Exact Mass ]:
774.160889

[ PSA ]:
82.64000

[ LogP ]:
19.48

[ Vapour Pressure ]:
0.0±1.9 mmHg at 25°C

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS06

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H301 + H311 + H331

[ Precautionary Statements ]:
P261-P280-P301 + P310-P311

[ RIDADR ]:
3146.0

[ Hazard Class ]:
6.1

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

4,8-Bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b']dithiophene
Trimethyltin chloride
2-Ethylhexyl bromide
Benzo[1,2-b;4,5-b']dithiophene-4,8-dione
2-ethylhexyl p-toluenesulfonate

DownStream

Articles

Synthesis of fluorinated polythienothiophene-co-benzodithiophenes and effect of fluorination on the photovoltaic properties.

J. Am. Chem. Soc. 133 , 1885-1894, (2011)

Herein, we describe the synthesis of fluorinated polythienothiophene-co-benzodithiophenes (PTBFs) and the characterization of their physical properties, especially their performance in solar cells. Fl...

Synthesis of conjugated polymers for organic solar cell applications.

Chem. Rev. 109(11) , 5868-5923, (2009)

Development of new semiconducting polymers for high performance solar cells.

J. Am. Chem. Soc. 1st ed., 131 , 56-57, (2009)

A new low band gap semiconducting polymer, PTB1, was synthesized and found promising for solar energy harvesting. Simple polymer solar cells based on PTB1 and methanofullerene [6,6]-phenyl-C(71)-butyr...

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