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1333488-67-7

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1333488-67-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1333488-67-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,4,8 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1333488-67:
(9*1)+(8*3)+(7*3)+(6*3)+(5*4)+(4*8)+(3*8)+(2*6)+(1*7)=167
167 % 10 = 7
So 1333488-67-7 is a valid CAS Registry Number.

1333488-67-7Downstream Products

1333488-67-7Relevant academic research and scientific papers

Boundaries of anion/naphthalenediimide interactions: From anion-π interactions to anion-induced charge-transfer and electron-transfer phenomena

Guha, Samit,Goodson, Flynt S.,Corson, Lucas J.,Saha, Sourav

, p. 13679 - 13691 (2012)

The recent emergence of anion-π interactions has added a new dimension to supramolecular chemistry of anions. Yet, after a decade since its inception, actual mechanisms of anion-π interactions remain highly debated. To elicit a complete and accurate understanding of how different anions interact with π-electron-deficient 1,4,5,8-naphthalenediimides (NDIs) under different conditions, we have extensively studied these interactions using powerful experimental techniques. Herein, we demonstrate that, depending on the electron-donating abilities (Lewis basicity) of anions and electron-accepting abilities (π-acidity) of NDIs, modes of anion-NDI interactions vary from extremely weak non-chromogenic anion-π interactions to chromogenic anion-induced charge-transfer (CT) and electron-transfer (ET) phenomena. In aprotic solvents, electron-donating abilities of anions generally follow their Lewis basicity order, whereas π-acidity of NDIs can be fine-tuned by installing different electron-rich and electron-deficient substituents. While strongly Lewis basic anions (OH- and F-) undergo thermal ET with most NDIs, generating NDI?- radical anions and NDI 2- dianions in aprotic solvents, weaker Lewis bases (AcO-, H2PO4-, Cl-, etc.) often require the photoexcitation of moderately π-acidic NDIs to generate the corresponding NDI?- radical anions via photoinduced ET (PET). Poorly Lewis basic I- does not participate in thermal ET or PET with most NDIs (except with strongly π-acidic core-substituted dicyano-NDI) but forms anion/NDI CT or anion-π complexes. We have looked for experimental evidence that could indicate alternative mechanisms, such as a Meisenheimer complex or CH anion hydrogen-bond formation, but none was found to support these possibilities.

Electronically regulated thermally and light-gated electron transfer from anions to naphthalenediimides

Guha, Samit,Goodson, Flynt S.,Roy, Sovan,Corson, Lucas J.,Gravenmier, Curtis A.,Saha, Sourav

supporting information; experimental part, p. 15256 - 15259 (2011/11/05)

Anion-induced electron transfer (ET) to π-electron-deficient naphthalenediimides (NDIs) can be channeled through two distinct pathways by adjusting the Lewis basicity of the anion and the π-acidity of the NDI: (1) When the anion and NDI are a strong elect

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