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Volumn 68, Issue 10, 2003, Pages 3947-3957

Molecular recognition of NO/NO+ via multicenter (charge-transfer) binding to bridged diarene donors. Effect of structure on the optical transitions and complexation thermodynamics

Author keywords

[No Author keywords available]

Indexed keywords

CHARGE TRANSFER; CHEMICAL SENSORS; ELECTRON TRANSITIONS; FREE ENERGY; NITROGEN OXIDES; REDOX REACTIONS;

EID: 0037951299     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo030015q     Document Type: Article
Times cited : (30)

References (84)
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    • In complexes with bis-coordinated nitrosonium, there are also transitions from the noninteracting orbitals of the arene to the antibonding molecular orbital; but they are expected to be much less intense (similar to the low-energy bands VL in 1:1 complexes) and are overshadowed by the nonbonding-to-antibonding transition.
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    • CT = -RT ln K) is considered instead of the equilibrium constant to allow direct comparison with different donor/acceptor stoichiometries.
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    • The energy (enthalpy) gain of [1:1] and [2:1] complexes is mainly connected with the relocation of two electrons initially residing on the donor orbital to lower-lying molecular orbitals of the complex. The second electron pair in [2:1] complexes resides on the nonbonding orbital.
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    • max at 380 and 780 nm).
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    • . in vacuo.
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    • 20 The problem is related to the apparent mismatch of the diarene cavity to the requirements of the guest.
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    • (a) Particularly in nonaqueous solutions.
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    • (b) Note that this procedure circumvents the kinetic lability of arene cation radicals.
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    • (c) From the results in Table 1 (eq 2), we estimate the intrinsic NO sensitivity to be ∼1 μM on the basis of a spectrophotometric resolution of 0.01 in the optical density; but for a solid-state device, the practical sensitivity will depend on its design, particularly for application to an aqueous environment.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.