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16004-75-4

  • Product Name:1,3,5,7-TETRAPHENYLADAMANTANE
  • Molecular Formula:C34H32
  • Molecular Weight:440.628
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Product Details

pd_meltingpoint:403-404 °C

Purity:99%

Reputable supplier selling 1,3,5,7-TETRAPHENYLADAMANTANE 16004-75-4 with stock

  • Molecular Formula:C34H32
  • Molecular Weight:440.628
  • Melting Point:403-404 °C 
  • Boiling Point:575.5±50.0 °C(Predicted) 
  • PSA：0.00000 
  • Density:1.174±0.06 g/cm3(Predicted) 
  • LogP:8.11980 

1,3,5,7-TETRAPHENYLADAMANTANE(Cas 16004-75-4) Usage

General Description

1,3,5,7-TETRAPHENYLADAMANTANE is a meta-substituted tetraaryl adamantane derivative that exhibits enhanced white-light emission properties compared to simpler adamantane structures, making it a promising candidate for optoelectronic applications. 1,3,5,7-TETRAPHENYLADAMANTANE's unique tetraaryl substitution pattern contributes to its highly directional emission when excited by a continuous wave laser diode.

InChI:InChI=1S/C34H32/c1-5-13-27(14-6-1)31-21-32(28-15-7-2-8-16-28)24-33(22-31,29-17-9-3-10-18-29)26-34(23-31,25-32)30-19-11-4-12-20-30/h1-20H,21-26H2

16004-75-4 Relevant articles

Novel sulfonate-containing halogen-free flame-retardants: Effect of ternary and quaternary sulfonates centered on adamantane on the properties of polycarbonate composites

Zhu, Dong Yu,Guo, Jian Wei,Xian, Jia Xing,Fu, Shu Qin

, p. 39270 - 39278 (2017)

In order to find a more environmentally ...

Design of solvatomorphic structures based on a polyboronated tetraphenyladamantane molecular tecton

Drapa?a, Jakub,Durka, Krzysztof,Gontarczyk, Krzysztof,Klimkowski, Piotr,Luliński, Sergiusz,Marek-Urban, Paulina H.,Urbanowicz, Karolina A.,Wo?niak, Krzysztof

, p. 8169 - 8182 (2021/12/08)

A series of solvatomorphic structures of...

Regioselective Synthesis of meta-Tetraaryl-Substituted Adamantane Derivatives and Evaluation of Their White Light Emission

Becker, Jonathan,Bernhardt, Bastian,Gowrisankar, Saravanan,Schreiner, Peter R.

supporting information, p. 6806 - 6810 (2021/12/31)

New meta-substituted tetraaryl adamantan...

Chromophore Multiplication To Enable Exciton Delocalization and Triplet Diffusion Following Singlet Fission in Tetrameric Pentacene

Hetzer, Constantin,Basel, Bettina S.,Kopp, Sebastian M.,Hampel, Frank,White, Fraser J.,Clark, Timothy,Guldi, Dirk M.,Tykwinski, Rik R.

supporting information, p. 15263 - 15267 (2019/10/22)

A tetrameric pentacene, PT, has been use...

Azo-linked porous organic polymers: Robust and time-efficient synthesis: Via NaBH4-mediated reductive homocoupling on polynitro monomers and adsorption capacity towards aniline in water

Zhou, Jin-Xiu,Luo, Xian-Sheng,Liu, Xiangxiang,Qiao, Yan,Wang, Pengfei,Mecerreyes, David,Bogliotti, Nicolas,Chen, Shi-Lu,Huang, Mu-Hua

supporting information, p. 5608 - 5612 (2018/04/12)

Time-efficient synthetic methods of poro...

16004-75-4 Process route

1-Adamantyl bromide
768-90-1

1-Adamantyl bromide

benzene
71-43-2,26181-88-4,54682-86-9,13967-78-7,174973-66-1

benzene

1,3,5,7-tetrakis(phenyl)adamantane
16004-75-4

1,3,5,7-tetrakis(phenyl)adamantane

Conditions
Conditions Yield
With aluminum (III) chloride; t-butyl bromide; for 3h; Reflux;
95%
With aluminum (III) chloride; t-butyl bromide; for 4h; Reflux;
90%
With aluminum (III) chloride; t-butyl bromide; at 0 ℃; for 5h; Inert atmosphere; Reflux;
90%
With aluminium trichloride; t-butyl bromide; for 2h; Heating;
77%
With aluminium trichloride; t-butyl bromide; Heating;
77%
With aluminum (III) chloride; t-butyl bromide; for 2h; Inert atmosphere; Reflux;
66%
With aluminum (III) chloride; t-butyl bromide; for 7h; Inert atmosphere; Cooling with ice; Reflux;
60%
With aluminum (III) chloride; t-butyl bromide; for 2h; Cooling with ice;
60%
1-Adamantyl bromide; With aluminum (III) chloride; Cooling with ice; Inert atmosphere;
benzene; With t-butyl bromide; In benzene; for 6h; Inert atmosphere; Cooling with ice; Reflux;
58%
With aluminum (III) chloride; t-butyl bromide; for 2h; Reflux; Inert atmosphere;
48.7%
With aluminum (III) chloride; t-butyl bromide;
44%
With aluminum (III) chloride; t-butyl bromide; at 90 ℃;
With aluminum (III) chloride;
1-Adamantyl bromide; benzene; With t-butyl bromide; at 55 ℃; for 0.166667h;
With aluminum (III) chloride; for 1h; Reflux;
With aluminum (III) chloride; t-butyl bromide; for 4h; Inert atmosphere; Reflux;
With aluminum (III) chloride; t-butyl bromide;
adamantane
281-23-2

adamantane

benzene
71-43-2,26181-88-4,54682-86-9,13967-78-7,174973-66-1

benzene

1,3,5,7-tetrakis(phenyl)adamantane
16004-75-4

1,3,5,7-tetrakis(phenyl)adamantane

Conditions
Conditions Yield
With aluminum (III) chloride; t-butyl bromide; at 20 ℃; for 16h; regioselective reaction;
85%

16004-75-4 Upstream products

  • 7314-86-5
    7314-86-5

    1,3,5,7-tetrabromoadamantane

  • 71-43-2
    71-43-2

    benzene

  • 768-90-1
    768-90-1

    1-Adamantyl bromide

  • 281-23-2
    281-23-2

    adamantane

16004-75-4 Downstream products

  • 16080-28-7
    16080-28-7

    1,3,5,7-Tetracyclohexyl-adamantan

  • 144970-30-9
    144970-30-9

    1,3,5,7-tetrakis(4-iodophenyl)adamantane

  • 144970-36-5
    144970-36-5

    1,3,5,7-tetrakis(4-bromophenyl)adamantane

  • 167013-23-2
    167013-23-2

    1,3,5,7-tetrakis-(4-cyanophenyl)adamantane

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