✦ LIBER ✦

Cyclic conjugation in dianions: effect of cycles on the thermodynamic stability of polycyclic conjugated dianions

✍ Scribed by Ivan Gutman

Book ID: 114142746
Publisher: Elsevier Science
Year: 1998
Tongue: English
Weight: 444 KB
Volume: 428
Category: Article
ISSN: 0166-1280
DOI: 10.1016/s0166-1280(97)00287-x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Effect of polyethylene glycol conjugatio

Effect of polyethylene glycol conjugation on the circulatory stability of plasma-derived human butyrylcholinesterase in mice

✍ Sun, Wei; Luo, Chunyuan; Tipparaju, Prasanthi; Doctor, Bhupendra P.; Saxena, Ash 📂 Article 📅 2013 🏛 Elsevier Science 🌐 English ⚖ 284 KB

Nanoparticles in Biology and Medicine Vo

Nanoparticles in Biology and Medicine Volume 274 || Effect of Gold Nanoparticle Conjugation on the Activity and Stability of Functional Proteins

✍ Soloviev, Mikhail 📂 Article 📅 2012 🏛 Humana Press ⚖ 362 KB

High-pressure and temperature effects on

High-pressure and temperature effects on the inactivation of Bacillus amyloliquefaciens, alkaline phosphatase and storage stability of conjugated linoleic acid in milk

✍ Martínez-Monteagudo, Sergio I.; Gänzle, Michael G.; Saldaña, Marleny D.A. 📂 Article 📅 2014 🏛 Elsevier Science 🌐 English ⚖ 354 KB

Structure–activity relationships in plat

Structure–activity relationships in platinum–acridinylthiourea conjugates: effect of the thiourea nonleaving group on drug stability, nucleobase affinity, and in vitro cytotoxicity

✍ Margaret C. Ackley; Colin G. Barry; Amanda M. Mounce; Michael C. Farmer; Beth-Er 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 307 KB

ChemInform Abstract: Effect of the α-Alk

ChemInform Abstract: Effect of the α-Alkyl Substituent of Conjugated Nitroolefins on the Formation of Cyclic Nitronic Esters vs. Nitrocyclopropanes in Their Reaction with Sulfur Ylides.

✍ G. KUMARAN; G. H. KULKARNI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB

Evaluation of the π-conjugative effect o

Evaluation of the π-conjugative effect of the 2-methylene and the 2-oxo substituent on the stability of carbocations in the solvolysis of bicyclic bridgehead derivatives

✍ Ken'ichi Takeuchi; Fumio Akiyama; Keizo Ikai; Tadashi Shibata; Midori Kato 📂 Article 📅 1988 🏛 Elsevier Science 🌐 French ⚖ 280 KB

The cyano and carbonyl groups are strongly electron withdrawing (-I). However. in recent years considerable experimental and theoretical efforts have been made in evaluating the ITconjugative electron donation (+M) of these substituents toward cationic carbon (schemes 1 and 2).' As for the effect of