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5-[4-(hexyloxy)phenyl]dipyrromethane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

500907-22-2

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500907-22-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 500907-22-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,9,0 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 500907-22:
(8*5)+(7*0)+(6*0)+(5*9)+(4*0)+(3*7)+(2*2)+(1*2)=112
112 % 10 = 2
So 500907-22-2 is a valid CAS Registry Number.

500907-22-2Relevant academic research and scientific papers

Stable negative differential resistance in porphyrin based σ-π-σ monolayers grafted on silicon

Garg, Kavita,Majumder, Chiranjib,Gupta, Shiv Kumar,Aswal, Dinesh Kumar,Nayak, Sandip Kumar,Chattopadhyay, Subrata

, p. 50234 - 50244 (2015/06/25)

Two Si-based hybrid self-assembled monolayers were synthesized by electro-grafting two di-O-alkylated porphyrins as the σ-π-σ systems. The monolayers showed a stable and reversible negative differential resistance (NDR) property at room temperature. The monolayer, fabricated using the porphyrin with fluorophenyl groups was more compact and showed a tenfold peak-to-valley ratio (PVR) relative to the other similar system devoid of the fluorine atoms in the porphyrin moiety. This suggested better pre-organization of the former, possibly by hydrogen bonding through the electro-negative fluorine atoms.

Molecular engineering of boryl oxasmaragdyrins through peripheral modification: Structure-efficiency relationship

Mane, Sandeep B.,Hung, Chen-Hsiung

, p. 4825 - 4841 (2015/03/18)

Expanded porphyrins with the absorption profile down to the infrared region through increased p-conjugation are suitable candidates for a low energy sensitizer. Oxasmaragdyrin boron complexes, a class of aromatic-coremodified expanded porphyrin with 22 π -electrons, have been recently utilized as an efficient low energy sensitizer in dye-sensitized solar cells. In this paper, we have prepared a series of eight novel boryl oxasmaragdyrins through molecular engineering on the periphery and their overall photovoltaic performances in dye-sensitized solar cells are evaluated. With the help of photophysical, electrochemical, and photovoltaic studies, it is revealed that molecular structure, especially the number and position of the donor-acceptor groups play a pivotal role in their photovoltaic performance. Presence of the two well-separated split Soret bands in the 400-500 nm region of UV/Vis spectrum ensures broader coverage of absorption wavelengths. Even though the two-an-choring-group dyes (SM5-SM8 ) bind strongly to TiO2 compared to one-anchoring-group dyes (SM1-SM4), the latter have superior photovoltaic performance than the former. Dye SM1 , with two hexyloxyphenyl donors and one carboxylic acid anchor showed the best overall conversion efficiency of 4.36% (JSC = 10.91 mAcm-2 ; VOC = 0.59 V; FF = 0.68). This effective modulation of photovoltaic performance through structural engineering of the dyes will serve as a guideline for the future design of efficient low energy light-harvesting sensitizers.

BODIPY-based conjugated polymers for broadband light sensing and harvesting applications

Cortizo-Lacalle, Diego,Howells, Calvyn T.,Gambino, Salvatore,Vilela, Filipe,Vobecka, Zuzana,Findlay, Neil J.,Inigo, Anto R.,Thomson, Stuart A. J.,Skabara, Peter J.,Samuel, Ifor D. W.

experimental part, p. 14119 - 14126 (2012/09/22)

The synthesis of novel low band-gap polymers has significantly improved light sensing and harvesting in polymer-fullerene devices. Here the synthesis of two low band-gap polymers based on the 4,4-difluoro-4-bora-3a,4a-diaza-s- indacene core (BODIPY), and

Design and synthesis of light-harvesting rods for intrinsic rectification of the migration of excited-state energy and ground-state holes

Loewe, Robert S.,Lammi, Robin K.,Diers, James R.,Kirmaier, Christine,Bocian, David F.,Holten, Dewey,Lindsey, Jonathan S.

, p. 1530 - 1552 (2007/10/03)

We present the design of molecular materials for ultimate use in solid-state solar cells. The molecular materials are semi-rigid oligomeric rods of defined length with metalloporphyrins in the backbone and a carboxy group at one end for attachment to a su

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