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molecular mechanics calculation (geometry optimization) forcite module, materials studio, version 5.5.3 (dassault systèmes co)  (Dassault Systemes)

 
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    Dassault Systemes molecular mechanics calculation (geometry optimization) forcite module, materials studio, version 5.5.3 (dassault systèmes co)
    Molecular Mechanics Calculation (Geometry Optimization) Forcite Module, Materials Studio, Version 5.5.3 (Dassault Systèmes Co), supplied by Dassault Systemes, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/forcite+geometry+optimization+module/molecular+mechanics+calculation++geometry+optimization++forcite+module++materials+studio++version+5+5+3++dassault+syst%C3%A8mes+co+/pm34133165-93-61-67
    Average 90 stars, based on 1 article reviews
    molecular mechanics calculation (geometry optimization) forcite module, materials studio, version 5.5.3 (dassault systèmes co) - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Nuclear Magnetic Resonance:

    Article Title: Supramolecular Singlet Fission of Pentacene Dimers within Polyaromatic Capsules.
    Article Snippet: We herein report a new set of supramolecular nanotools for the generation and modulation of singlet fission (SF) of noncovalent/ covalent pentacene dimers.. Two molecules of a pentacene monomer with bulky substituents are facilely encapsulated by a polyaromatic capsule, composed of naphthalene-based bent amphiphiles, in water.. The encapsulated noncovalent dimer converts to otherwise undetectable triplet pairs and an individual triplet in high quantum yields (179% and 53%, respectively) even under high dilution conditions.

    Fluorescence:

    Article Title: Supramolecular Singlet Fission of Pentacene Dimers within Polyaromatic Capsules.
    Article Snippet: We herein report a new set of supramolecular nanotools for the generation and modulation of singlet fission (SF) of noncovalent/ covalent pentacene dimers.. Two molecules of a pentacene monomer with bulky substituents are facilely encapsulated by a polyaromatic capsule, composed of naphthalene-based bent amphiphiles, in water.. The encapsulated noncovalent dimer converts to otherwise undetectable triplet pairs and an individual triplet in high quantum yields (179% and 53%, respectively) even under high dilution conditions.

    Particle Size Analysis:

    Article Title: Supramolecular Singlet Fission of Pentacene Dimers within Polyaromatic Capsules.
    Article Snippet: We herein report a new set of supramolecular nanotools for the generation and modulation of singlet fission (SF) of noncovalent/ covalent pentacene dimers.. Two molecules of a pentacene monomer with bulky substituents are facilely encapsulated by a polyaromatic capsule, composed of naphthalene-based bent amphiphiles, in water.. The encapsulated noncovalent dimer converts to otherwise undetectable triplet pairs and an individual triplet in high quantum yields (179% and 53%, respectively) even under high dilution conditions.

    Dynamic Light Scattering Assay:

    Article Title: Supramolecular Singlet Fission of Pentacene Dimers within Polyaromatic Capsules.
    Article Snippet: We herein report a new set of supramolecular nanotools for the generation and modulation of singlet fission (SF) of noncovalent/ covalent pentacene dimers.. Two molecules of a pentacene monomer with bulky substituents are facilely encapsulated by a polyaromatic capsule, composed of naphthalene-based bent amphiphiles, in water.. The encapsulated noncovalent dimer converts to otherwise undetectable triplet pairs and an individual triplet in high quantum yields (179% and 53%, respectively) even under high dilution conditions.

    Lyophilization:

    Article Title: Supramolecular Singlet Fission of Pentacene Dimers within Polyaromatic Capsules.
    Article Snippet: We herein report a new set of supramolecular nanotools for the generation and modulation of singlet fission (SF) of noncovalent/ covalent pentacene dimers.. Two molecules of a pentacene monomer with bulky substituents are facilely encapsulated by a polyaromatic capsule, composed of naphthalene-based bent amphiphiles, in water.. The encapsulated noncovalent dimer converts to otherwise undetectable triplet pairs and an individual triplet in high quantum yields (179% and 53%, respectively) even under high dilution conditions.



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